When you publish results in the scientific literature that were obtained with programs of the ADF package, you are required to include references to the program package with the appropriate release number, and a few key publications.
In addition to these general references, references to special features are mandatory, in case you have used them. See the section Feature References ADF and Feature References BAND.
For ReaxFF calculations, include the relevant Force Field Reference in addition to the general ReaxFF references.
For calculations with the molecular ADF program, version 2012:
1. G. te Velde, F.M. Bickelhaupt, S.J.A. van Gisbergen, C. Fonseca Guerra, E.J. Baerends, J.G. Snijders and T. Ziegler, Chemistry with ADF. Journal of Computational Chemistry 22, 931 (2001)
2. C. Fonseca Guerra, J.G. Snijders, G. te Velde and E.J. Baerends, Towards an order-N DFT method. Theoretical Chemistry Accounts 99, 391 (1998)
3. ADF2012, SCM, Theoretical Chemistry, Vrije Universiteit,
Amsterdam, The Netherlands, http://www.scm.com
Optionally, you may add the following list of authors and contributors:
E.J. Baerends, T. Ziegler, J. Autschbach, D. Bashford, A. Bérces, F.M. Bickelhaupt, C. Bo, P.M. Boerrigter, L. Cavallo,
D.P. Chong, L. Deng, R.M. Dickson, D.E. Ellis, M. van Faassen,
L. Fan, T.H. Fischer, C. Fonseca Guerra, A. Ghysels, A. Giammona, S.J.A. van Gisbergen, A.W. Götz,
J.A. Groeneveld, O.V. Gritsenko, M. Grüning, S. Gusarov, F.E. Harris, P. van den Hoek,
C.R. Jacob, H. Jacobsen, L. Jensen, J.W. Kaminski, G. van Kessel, F. Kootstra, A. Kovalenko, M.V. Krykunov, E. van Lenthe, D.A. McCormack,
A. Michalak, M. Mitoraj, J. Neugebauer, V.P. Nicu, L. Noodleman, V.P. Osinga,
S. Patchkovskii, P.H.T. Philipsen, D. Post, C.C. Pye, W. Ravenek, J.I. Rodríguez,
P. Ros, P.R.T. Schipper,
G. Schreckenbach, J.S. Seldenthuis, M. Seth, J.G. Snijders, M. Solà, M. Swart, D. Swerhone,
G. te Velde, P. Vernooijs, L. Versluis, L. Visscher, O. Visser, F. Wang, T.A. Wesolowski, E.M. van Wezenbeek,
G. Wiesenekker, S.K. Wolff, T.K. Woo, A.L. Yakovlev
Note: if you have used a modified (by yourself, for instance) version of the code, you should mention in the citation that a modified version has been used.
For calculations with the periodic structures BAND program, version 2012:
1. G. te Velde and E.J. Baerends, Precise density-functional method for periodic structures. Physical Review B 44, 7888 (1991)
2. G. Wiesenekker and E.J. Baerends, Quadratic integration over the three-dimensional Brillouin zone. Journal of Physics: Condensed Matter 3, 6721 (1991)
3. BAND2012, SCM, Theoretical Chemistry, Vrije Universiteit,
Amsterdam, The Netherlands, http://www.scm.com
Optionally, you may add the following list of authors and contributors:
P.H.T. Philipsen, G. te Velde, E.J. Baerends,
J.A. Berger, P.L. de Boeij, J.A. Groeneveld, E.S. Kadantsev, R. Klooster, F. Kootstra, P. Romaniello, D.G. Skachkov, J.G. Snijders,
G. Wiesenekker, T. Ziegler
Note: if you have used a modified (by yourself, for instance) version of the code, you should mention in the citation that a modified version has been used.
For calculations with the Density Functional Tight Binding (DFTB) program:
1. ADF DFTB 2012, SCM, Theoretical Chemistry, Vrije Universiteit,
Amsterdam, The Netherlands, http://www.scm.com
Optionally, you may add the following list of authors and contributors:
Stefano Borini, Pier Philipsen, Alexei Yakovlev, Drew McCormack, Serguei Patchkovskii, Thomas Heine
If you use one of the included parameter sets you must also add the proper reference for it.
For calculations with MOPAC:
1. MOPAC2009, J. J. P. Stewart, Stewart Computational Chemistry; Colorado Springs, CO, USA
2. J. J. P. Stewart,
Optimization of Parameters for Semiempirical Methods V: Modification of NDDO Approximations and Application to 70 Elements.,
J. Mol. Model. 13, 1173-1213 (2007)
For calculations with the COSMO-RS program, version 2012:
1. C.C. Pye, T. Ziegler, E. van Lenthe, J.N. Louwen, An implementation of the conductor-like screening model of solvation within the Amsterdam density functional package. Part II. COSMO for real solvents. Can. J. Chem. 87, 790 (2009)
2. ADF2012 COSMO-RS, SCM, Theoretical Chemistry, Vrije Universiteit,
Amsterdam, The Netherlands, http://www.scm.com
Optionally, you may add the following list of authors and contributors:
J.N. Louwen, C.C. Pye, E. van Lenthe, E.S. McGarrity
The ReaxFF software that SCM makes available is based on the ReaxFF program developed by Adri van Duin.
For calculations with ReaxFF:
1. A.C.T. van Duin, S. Dasgupta, F. Lorant, and W. A. Goddard, ReaxFF: A reactive force field for hydrocarbons. Journal of Physical Chemistry A 105, 9396-9409 (2001)
2. K. Chenoweth, A.C.T. van Duin, and W.A. Goddard, ReaxFF reactive force field for molecular dynamics simulations of hydrocarbon oxidation. Journal of Physical Chemistry A 112, 1040-1053 (2008)
3. ReaxFF 2012, SCM, Theoretical Chemistry, Vrije Universiteit,
Amsterdam, The Netherlands, http://www.scm.com
Optionally, you may add the following list of authors and contributors:
A.C.T. van Duin, W.A. Goddard
The ReaxFF GUI (ReaxFFinput and ADFmovie) has been developed within SCM (with O. Visser as primary developer).
The ReaxFF program has been optimized (much faster, running in parallel, and using shared memory) by SCM (with A.L. Yakovlev as primary developer).
If you use one of the included force fields you must also add the proper reference for it .
Many examples of ReaxFF applications can be found on Prof. van Duin's publication list.
The integrated GUI has been developed by SCM (with O. Visser as primary developer), with some contributions from outside SCM (especially P. Leyronnas, W.-J. van Zeist, and M. Luppi).
If you used the GUI you may optionally include the reference:
GUI 2012, SCM, Amsterdam, The Netherlands, http://www.scm.com
For calculations with the Quild program
M. Swart and F.M. Bickelhaupt, QUILD: QUantum-regions interconnected by local descriptions. Journal of Computational Chemistry 29, 724 (2007)
For calculations with PyMD:
1. PyMD 2012, SCM,
R. E. Bulo, C. R. Jacob, S. Borini,
A python library for flexible multi-scale molecular dynamics simulations.
http://www.scm.com
When you have used special features, you should include one (or more, as the case may be) lead reference(s) to the implementation. Additional references to related publications are suggested.
E. van Lenthe and E.J. Baerends, Optimized Slater-type basis sets for the elements 1-118. Journal of Computational Chemistry 24, 1142 (2003)
spherical Gaussian nuclear charge distribution model
J. Autschbach, Magnitude of Finite-Nucleus-Size Effects in Relativistic Density Functional Computations of Indirect NMR Nuclear Spin-Spin Coupling Constants. ChemPhysChem 10, 2274 (2009)
L. Versluis and T. Ziegler, The determination of Molecular Structure by Density Functional Theory. Journal of Chemical Physics 88, 322 (1988)
L. Fan and T. Ziegler, Nonlocal density functional theory as a practical tool in calculations on transition states and activation energies. Journal of the American Chemical Society 114, 10890 (1992)
L. Deng, T. Ziegler and L. Fan, A combined density functional and intrinsic reaction coordinate study on the ground state energy surface of H2CO. Journal of Chemical Physics 99, 3823 (1993)
L. Deng and T. Ziegler, The determination of Intrinsic Reaction Coordinates by density functional theory. International Journal of Quantum Chemistry 52, 731 (1994)
G. Henkelman, B.P. Uberuaga and H. Jónsson, A climbing image nudged elastic band method for finding saddle points and minimum energy paths. Journal of Chemical Physics 113, 9901 (2000)
M. Krykunov and T. Ziegler, On the use of the exact exchange optimized effective potential method for static response properties, International Journal of Quantum Chemistry 109, 3246 (2009)
Lead references
E. van Lenthe, E.J. Baerends and J.G. Snijders, Relativistic regular two-component Hamiltonians. Journal of Chemical Physics 99, 4597 (1993)
E. van Lenthe, E.J. Baerends and J.G. Snijders, Relativistic total energy using regular approximations. Journal of Chemical Physics 101, 9783 (1994)
E. van Lenthe, A.E. Ehlers and E.J. Baerends, Geometry optimization in the Zero Order Regular Approximation for relativistic effects. Journal of Chemical Physics 110, 8943 (1999)
Suggested related references
E. van Lenthe, J.G. Snijders and E.J. Baerends, The zero-order regular approximation for relativistic effects: The effect of spin.orbit coupling in closed shell molecules. Journal of Chemical Physics 105, 6505 (1996)
E. van Lenthe, R. van Leeuwen, E.J. Baerends and J.G. Snijders, Relativistic regular two-component Hamiltonians. International Journal of Quantum Chemistry 57, 281 (1996)
Lead references
J.G. Snijders, E.J. Baerends and P. Ros, A perturbation theory approach to relativistic calculations. II. Molecules. Molecular Physics 38, 1909 (1979)
P.M. Boerrigter, E.J. Baerends and J.G. Snijders, A relativistic LCAO Hartree-Fock-Slater investigation of the electronic structure of the actinocenes M(COT)2, M=Th, Pa, U, Np and Pu. Chemical Physics 122, 357 (1988)
T. Ziegler, V. Tschinke, E.J. Baerends, J.G. Snijders and W. Ravenek, Calculation of bond energies in compounds of heavy elements by a quasi-relativistic approach. Journal of Physical Chemistry 93, 3050 (1989)
C.C. Pye and T. Ziegler, An implementation of the conductor-like screening model of solvation within the Amsterdam density functional package. Theoretical Chemistry Accounts 101, 396 (1999)
Lead
T. K. Woo, L. Cavallo and T. Ziegler, Implementation of the IMOMM methodology for performing combined QM/MM molecular dynamics simulations and frequency calculations. Theoretical Chemistry Accounts 100, 307 (1998)
Suggested
T. K. Woo, S. Patchkovskii, and T. Ziegler, Atomic Scale Modeling of Polymerization Catalysts. Computing in Science & Engineering, 2, 28-37 (2000)
For AddRemove model
M. Swart, AddRemove: A new link model for use in QM/MM studies. International Journal of Quantum Chemistry 91, 177 (2003)
T.A. Wesolowski and A. Warshel, Frozen Density Functional Approach for ab-initio Calculations of Solvated Molecules. Journal of Physical Chemistry 97, 8050 (1993)
J. Neugebauer, C.R. Jacob, T.A. Wesolowski and E.J. Baerends, An Explicit Quantum Chemical Method for Modeling Large Solvation Shells Applied to Aminocoumarin C151. Journal of Physical Chemistry A 109, 7805 (2005)
C.R. Jacob, J. Neugebauer and L. Visscher, A flexible implementation of frozen-density embedding for use in multilevel simulations. Journal of Computational Chemistry 29, 1011 (2008)
L. Jensen, P.T. van Duijnen and J.G. Snijders, A discrete solvent reaction field model within density functional theory. Journal of Chemical Physics 118, 514 (2003)
J.L. Chen, L. Noodleman, D.A. Case and D. Bashford, Incorporating solvation effects into density functional electronic structure calculations, Journal of Physical Chemistry 98, 11059 (1994)
VSCRF (vertical excitation self-consistent reaction field)
T. Liu, W.-G Han, F. Himo, G.M. Ullmann, D. Bashford, A. Toutchkine, K.M. Hahn, and L. Noodleman, Density Functional Vertical Self-Consistent Reaction Field Theory for Solvatochromism Studies of Solvent-Sensitive Dyes. Journal of Physical Chemistry A 108, 3545 (2004)
W.-G. Han, T. Liu, F. Himo, A. Toutchkine, D. Bashford, K.M. Hahn, L. Noodleman, A Theoretical Study of the UV/Visible Absorption and Emission Solvatochromic Properties of Solvent-Sensitive Dyes. ChemPhysChem 4, 1084 (2003)
Lead
S. Gusarov, T. Ziegler, and A. Kovalenko, Self-Consistent Combination of the Three-Dimensional RISM Theory of Molecular Solvation with Analytical Gradients and the Amsterdam Density Functional Package, Journal of Physical Chemistry A 110, 6083 (2006)
Suggested
A. Kovalenko and F. Hirata, Self-consistent description of a metal-water interface by the Kohn-Sham density functional theory and the three-dimensional reference interaction site model, Journal of Chemical Physics 110, 10095 (1999)
A. Kovalenko, Three-dimensional RISM theory for molecular liquids and solid-liquid interfaces., In Molecular Theory of Solvation; Hirata, Fumio, Ed.; Understanding Chemical Reactivity (series); Mezey, Paul G., Series Ed.; Kluwer Acadamic Publishers: Dordrecht, The Netherlands, 2003; Vol. 24, pp 169-275.
S. Grimme, Semiempirical GGA-Type Density Functional Constructed with a Long-Range Dispersion Correction. Journal of Computational Chemistry 27, 1787 (2006)
old implementation
S. Grimme, Accurate description of van der Waals complexes by density functional theory including empirical corrections. Journal of Computational Chemistry 25, 1463 (2004)
J.-M. Ducéré and L. Cavallo,
Parametrization of an Empirical Correction Term to Density Functional Theory for an Accurate Description of pi-Stacking Interactions in Nucleic Acids.
Journal of Physical Chemistry B 111, 13124 (2007)
contact: J.M. Ducere, L. Cavallo, University of Salerno, Italy
L. Fan and T. Ziegler, Application of density functional theory to infrared absorption intensity calculations on main group molecules. Journal of Chemical Physics 96, 9005 (1992)
L. Fan and T. Ziegler, Application of density functional theory to infrared absorption intensity calculations on transition-metal carbonyls. Journal of Physical Chemistry 96, 6937 (1992)
A. Bérces, R. M. Dickson, L. Fan, H. Jacobsen, D. Swerhone and T. Ziegler, An implementation of the coupled perturbed Kohn-Sham equations: perturbation due to nuclear displacements. Computer Physics Communications 100, 247 (1997)
H. Jacobsen, A. Bérces, D. Swerhone and T. Ziegler, Analytic second derivatives of molecular energies: a density functional implementation. Computer Physics Communications 100, 263 (1997)
S. K. Wolff, Analytical second derivatives in the Amsterdam density functional package. International Journal of Quantum Chemistry 104, 645 (2005)
Lead
A. Ghysels, D. Van Neck, V. Van Speybroeck, T. Verstraelen and M. Waroquier, Vibrational Modes in partially optimized molecular systems Journal of Chemical Physics126, 224102 (2007)
Suggested
A. Ghysels, D. Van Neck and M. Waroquier, Cartesian formulation of the Mobile Block Hessian Approach to vibrational analysis in partially optimized systems Journal of Chemical Physics127, 164108 (2007)
Raman scattering
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Application of time-dependent density functional response theory to Raman scattering. Chemical Physics Letters 259, 599 (1996)
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Implementation of time-dependent density functional response equations . Computer Physics Communications 118, 119 (1999)
Resonance Raman: excited-state finite lifetime
L. Jensen, L. Zhao, J. Autschbach and G.C. Schatz, Theory and method for calculating resonance Raman scattering from resonance polarizability derivatives, Journal of Chemical Physics 123, 174110 (2005)
Resonance Raman: excited-state gradient
J. Neugebauer, E.J. Baerends, E. Efremov, F. Ariese and C. Gooijer, Combined Theoretical and Experimental Deep-UV Resonance Raman Studies of Substituted Pyrenes. Journal of Physical Chemistry A 109, 2100 (2005)
L. Jensen, J. Autschbach, M. Krykunov, and G.C. Schatz, Resonance vibrational Raman optical activity: A time-dependent density functional theory approach, Journal of Chemical Physics 127, 134101 (2007)
V.P. Nicu J. Neugebauer S.K. Wolff and E.J. Baerends, A vibrational circular dichroism implementation within a Slater-type-orbital based density functional framework and its application to hexa- and hepta-helicenes. Theoretical Chemical Accounts 119, 245 (2008)
J.S. Seldenthuis, H.S.J. van der Zant, M.A. Ratner and J.M. Thijssen, Vibrational Excitations in Weakly Coupled Single-Molecule Junctions: A Computational Analysis. ACS Nano 2, 1445 (2008)
For all Time-Dependent DFT features (Excitation Energies, (Hyper) Polarizabilities, Dispersion Coefficients, Raman Scattering, include:
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Implementation of time-dependent density functional response equations . Computer Physics Communications 118, 119 (1999)
Lead reference
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Implementation of time-dependent density functional response equations . Computer Physics Communications 118, 119 (1999)
Suggested (when ZORA relativistic results are used)
A. Rosa, E.J. Baerends, S.J.A. van Gisbergen, E. van Lenthe, J.A. Groeneveld and J. G. Snijders, Article Electronic Spectra of M(CO)6 (M = Cr, Mo, W) Revisited by a Relativistic TDDFT Approach. Journal of the American Chemical Society 121, 10356 (1999)
Open Shell ground state
F. Wang and T. Ziegler, Mol. Phys.102, 2585 (2004)
Spin-flip transitions
F. Wang and T. Ziegler, Time-dependent density functional theory based on a noncollinear formulation of the exchange-correlation potential. Journal of Chemical Physics 121, 12191 (2004)
F. Wang and T. Ziegler, The performance of time-dependent density functional theory based on a noncollinear exchange-correlation potential in the calculations of excitation energies. Journal of Chemical Physics 122, 74109 (2005)
Core excitations
M. Stener, G. Fronzoni and M. de Simone, Time dependent density functional theory of core electrons excitations. Chemical Physics Letters 373, 115 (2003)
Excitations including spin-orbit coupling
F. Wang, T. Ziegler, E. van Lenthe, S.J.A. vand Gisbergen and E.J. Baerends, The calculation of excitation energies based on the relativistic two-component zeroth-order regular approximation and time-dependent density-functional with full use of symmetry. Journal of Chemical Physics 122, 204103 (2005)
Perturbative approach to include spin-orbit coupling
F. Wang and T. Ziegler, A simplified relativistic time-dependent density-functional theory formalism for the calculations of excitation energies including spin-orbit coupling effect, Journal of Chemical Physics 123, 154102 (2005)
M. Seth, G. Mazur, and T. Ziegler, Time-dependent density functional theory gradients in the Amsterdam density functional package: geometry optimizations of spin-flip excitations, Theoretical Chemistry Accounts 129, 331 (2011)
Lead
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, A Density Functional Theory study of frequency-dependent polarizabilities and van der Waals dispersion coefficients for polyatomic molecules. Journal of Chemical Physics 103, 9347 (1995)
Polarizabilities including spin-orbit coupling
A. Devarajan, A. Gaenko, and J. Autschbach, Two-component relativistic density functional method for computing nonsingular complex linear response of molecules based on the zeroth order regular approximation, Journal of Chemical Physics 130, 194102 (2009)
Suggested
V.P. Osinga, S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Density functional results for isotropic and anisotropic multipole polarizabilities and C6, C7, and C8 Van der Waals dispersion coefficients for molecules. Journal of Chemical Physics 106, 5091 (1997)
Lead
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Calculating frequency-dependent hyperpolarizabilities using time-dependent density functional theory. Journal of Chemical Physics 109, 10644 (1998)
Suggested:
S.J.A. van Gisbergen, J.G. Snijders, and E.J. Baerends, Time-dependent Density Functional Results for the Dynamic Hyperpolarizability of C60. Physical Review Letters 78, 3097 (1997)
Lead
V.P. Osinga, S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, Density functional results for isotropic and anisotropic multipole polarizabilities and C6, C7, and C8 Van der Waals dispersion coefficients for molecules. Journal of Chemical Physics 106, 5091 (1997)
Suggested
S.J.A. van Gisbergen, J.G. Snijders and E.J. Baerends, A Density Functional Theory study of frequency-dependent polarizabilities and van der Waals dispersion coefficients for polyatomic molecules. Journal of Chemical Physics 103, 9347 (1995)
Lead
J. Autschbach and T. Ziegler, Calculating molecular electric and magnetic properties from time-dependent density functional response theory. Journal of Chemical Physics 116, 891 (2002)
J. Autschbach, T. Ziegler, S.J.A. van Gisbergen and E.J. Baerends, Chiroptical properties from time-dependent density functional theory. I. Circular dichroism spectra of organic molecules. Journal of Chemical Physics 116, 6930 (2002)
Lead
J. Autschbach and T. Ziegler, Calculating molecular electric and magnetic properties from time-dependent density functional response theory. Journal of Chemical Physics 116, 891 (2002)
J. Autschbach, S. Patchkovskii, T. Ziegler, S.J.A. van Gisbergen and E.J. Baerends, Chiroptical properties from time-dependent density functional theory. II. Optical rotations of small to medium sized organic molecules. Journal of Chemical Physics 117, 581 (2002)
Lead
M. Krykunov and J. Autschbach, Calculation of static and dynamic linear magnetic response in approximate time-dependent density functional theory. Journal of Chemical Physics 126, 24101 (2007)
M. Seth, M. Krykunov, T. Ziegler, J. Autschbach and A. Banerjee, Application of magnetically perturbed time-dependent density functional theory to magnetic circular dichroism: Calculation of B terms, Journal of Chemical Physics 128, 144105 (2008)
M. Seth, M. Krykunov, T. Ziegler and J. Autschbach, Application of magnetically perturbed time-dependent density functional theory to magnetic circular dichroism. II. Calculation of A terms, Journal of Chemical Physics 128, 234102 (2008)
M. Seth, T. Ziegler and J. Autschbach, Application of magnetically perturbed time-dependent density functional theory to magnetic circular dichroism. III. Temperature-dependent magnetic circular dichroism induced by spin-orbit coupling, Journal of Chemical Physics 129, 104105 (2008)
M. Krykunov, A. Banerjee, T. Ziegler and J. Autschbach, Calculation of Verdet constants with time-dependent density functional theory. Implementation and results for small molecules, Journal of Chemical Physics 122, 074105 (2005)
M. Krykunov, M. Seth, T. Ziegler and J. Autschbach, Calculation of the magnetic circular dichroism B term from the imaginary part of the Verdet constant using damped time-dependent density functional theory, Journal of Chemical Physics 127, 244102 (2007)
Lead reference
G. Schreckenbach and T. Ziegler, The calculation of NMR shielding tensors using GIAO's and modern density functional theory. Journal of Physical Chemistry 99, 606 (1995)
NMR chemical shifts with hybrid functionals
M. Krykunov, T. Ziegler and E. van Lenthe, Hybrid density functional calculations of nuclear magnetic shieldings using Slater-type orbitals and the zeroth-order regular approximation. International Journal of Quantum Chemistry 109, 1676 (2009)
NMR chemical shifts with NBO analysis
J. Autschbach and S. Zheng, Analyzing Pt chemical shifts calculated from relativistic density functional theory using localized orbitals: The role of Pt 5d lone pairs, Magnetic Resonance in Chemistry 46, S45 (2008)
J. Autschbach, Analyzing NMR shielding tensors calculated with two-component relativistic methods using spin-free localized molecular orbitals, Journal of Chemical Physics 128, 164112 (2008)
Paramagnetic NMR chemical shifts
J. Autschbach, S. Patchkovskii, and B. Pritchard, Calculation of Hyperfine Tensors and Paramagnetic NMR Shifts Using the Relativistic Zeroth-Order Regular Approximation and Density Functional Theory. Journal of Chemical Theory and Computation 7, 2175 (2011)
Suggested
G. Schreckenbach and T. Ziegler, The calculation of NMR shielding tensors based on density functional theory and the frozen-core approximation. International Journal of Quantum Chemistry 60, 753 (1996)
G. Schreckenbach and T. Ziegler, Calculation of NMR shielding tensors based on density functional theory and a scalar relativistic Pauli-type Hamiltonian. The application to transition metal complexes. International Journal of Quantum Chemistry 61, 899 (1997)
S.K. Wolff and T. Ziegler, Calculation of DFT-GIAO NMR shifts with inclusion of spin-orbit coupling. Journal of Chemical Physics 109, 895 (1998)
S.K. Wolff, T. Ziegler, E. van Lenthe and E.J. Baerends, Density functional calculations of nuclear magnetic shieldings using the zeroth-order regular approximation (ZORA) for relativistic effects: ZORA nuclear magnetic resonance. Journal of Chemical Physics 110, 7689 (1999)
Lead
J. Autschbach and T. Ziegler, Nuclear spin-spin coupling constants from regular approximate density functional calculations. I. Formalism and scalar relativistic results for heavy metal compounds. Journal of Chemical Physics 113, 936 (2000)
J. Autschbach, and T. Ziegler, Nuclear spin-spin coupling constants from regular approximate relativistic density functional calculations. II. Spin-orbit coupling effects and anisotropies. Journal of Chemical Physics 113, 9410 (2000)
NMR spin-spin couplings with PBE0
J. Autschbach, Two-component relativistic hybrid density functional computations of nuclear spin-spin coupling tensors using Slater-type basis sets and density-fitting techniques. Journal of Chemical Physics 129, 094105 (2008), Erratum: Journal of Chemical Physics 130, 209901 (2009)
NMR spin-spin couplings with NBO analysis
J. Autschbach, Analyzing molecular properties calculated with two-component relativistic methods using spin-free Natural Bond Orbitals: NMR spin-spin coupling constants Journal of Chemical Physics 127, 124106 (2007)
Suggested
R.M. Dickson and T. Ziegler, NMR Spin.Spin Coupling Constants from Density Functional Theory with Slater-Type Basis Functions. Journal of Physical Chemistry 100, 5286 (1996)
J. Khandogin and T. Ziegler, A density functional study of nuclear magnetic resonance spin.spin coupling constants in transition-metal systems. Spectrochimica Acta 55, 607 (1999)
J. Autschbach and T. Ziegler, Solvent Effects on Heavy Atom Nuclear Spin.Spin Coupling Constants: A Theoretical Study of Hg.C and Pt.P Couplings. Journal of the American Chemical Society 123, 3341 (2001)
J. Autschbach and T. Ziegler, A Theoretical Investigation of the Remarkable Nuclear Spin.Spin Coupling Pattern in [(NC)5Pt-Tl(CN)]-. Journal of the American Chemical Society 123, 5320 (2001)
Suggested book reference
J. Autschbach, T. Ziegler, in Encyclopedia of Nuclear Magnetic Resonance, Eds. D.M. Grant, R. K. Harris, John Wiley and Sons, Chichester, 2002, Vol. 9 Advances in NMR.
Lead reference (self-consistent spin-orbit coupling)
E. van Lenthe, A. van der Avoird and P.E.S. Wormer, Density functional calculations of molecular g-tensors in the zero order regular approximation for relativistic effects. Journal of Chemical Physics 107, 2488 (1997)
Lead reference (perturbative inclusion spin-orbit coupling)
J. Autschbach and B. Pritchard, Calculation of molecular g-tensors using the zeroth-order regular approximation and density functional theory: expectation value versus linear response approaches . Theoretical Chemistry Accounts 129, 453 (2011)
Lead references (perturbative inclusion spin-orbit coupling with EPR/NMR program)
G. Schreckenbach and T. Ziegler, Calculation of the G-tensor of electron paramagnetic resonance spectroscopy using Gauge-Including Atomic Orbitals and Density Functional Theory. Journal of Physical Chemistry A 101, 3388 (1997) (for ESR/EPR g-tensor)
S. Patchkovskii and T. Ziegler, Calculation of the EPR g-Tensors of High-Spin Radicals with Density Functional Theory. Journal of Physical Chemistry A 105, 5490 (2001) (for high-spin ESR/EPR g-tensor)
Lead reference
E. van Lenthe, A. van der Avoird and P.E.S. Wormer, Density functional calculations of molecular hyperfine interactions in the zero order regular approximation for relativistic effects. Journal of Chemical Physics 108, 4783 (1998)
Lead reference (perturbative inclusion spin-orbit coupling)
J. Autschbach, S. Patchkovskii, and B. Pritchard, Calculation of Hyperfine Tensors and Paramagnetic NMR Shifts Using the Relativistic Zeroth-Order Regular Approximation and Density Functional Theory. Journal of Chemical Theory and Computation 7, 2175 (2011)
Lead reference (in ESR called Q-tensor: Nuclear electric quadrupole hyperfine interaction)
E. van Lenthe and E.J. Baerends, Density functional calculations of nuclear quadrupole coupling constants in the zero-order regular approximation for relativistic effects. Journal of Chemical Physics 112, 8279 (2000)
EFG with NBO analysis
A.J. Rossini, R.W. Mills, G.A. Briscoe, E.L. Norton, S.J. Geier, I. Hung, S. Zheng, J. Autschbach, and R.W. Schurko, Solid-State Chlorine NMR of Group IV Transition Metal Organometallic Complexes, Journal of the American Chemical Society 131, 3317 (2009)
J. Autschbach, S. Zheng, and R.W. Schurko, Analysis of Electric Field Gradient Tensors at Quadrupolar Nuclei in Common Structural Motifs, Concepts in Magnetic Resonance Part A 36A, 84 (2010)
Chapter 2 and appendix C of
J.S. Seldenthuis,
Electrical and mechanical effects in single-molecule junctions,
PhD thesis, Delft University of Technology, 2011
T. Ziegler and A. Rauk, A theoretical study of the ethylene-metal bond in complexes between Cu+, Ag+, Au+, Pt0 or Pt2+ and ethylene, based on the Hartree-Fock-Slater transition-state method. Inorganic Chemistry 18, 1558 (1979)
T. Ziegler and A. Rauk, Carbon monoxide, carbon monosulfide, molecular nitrogen, phosphorus trifluoride, and methyl isocyanide as sigma donors and pi acceptors. A theoretical study by the Hartree-Fock-Slater transition-state method. Inorganic Chemistry 18, 1755 (1979)
F.M. Bickelhaupt and E.J. Baerends, In: Rev. Comput. Chem.; K.B. Lipkowitz and D.B. Boyd, Eds.; Wiley, New York, 2000, Vol. 15, p.1-86
M. Mitoraj, A. Michalak and T. Ziegler, A Combined Charge and Energy Decomposition Scheme for Bond Analysis, Journal of Chemical Theory and Computation 5, 962 (2009)
Grid-based algorithm
J.I. Rodríguez, R.F.W. Bader, P.W. Ayers, C. Michel, A.W. Götz and C. Bo, A high performance grid-based algorithm for computing QTAIM properties. Chemical Physics Letters 472, 149 (2009)
Lead
See key references above, for all work with BAND
Suggested
G. Wiesenekker, G. te Velde and E.J. Baerends, Analytic quadratic integration over the two-dimensional Brillouin zone. Journal of Physics C: Solid State Physics 21, 4263 (1988)
G. te Velde and E.J. Baerends, Numerical integration for polyatomic systems. Journal of Computational Physics 99, 84 (1992)
Lead
E.S. Kadantsev, R. Klooster. P.L. de Boeij and T. Ziegler, The Formulation and Implementation of Analytic Energy Gradients for Periodic Density Functional Calculations with STO/NAO Bloch Basis Set. Molecular Physics 105, 2583 (2007)
Lead
F. Kootstra, P.L. de Boeij and J.G. Snijders, Efficient real-space approach to time-dependent density functional theory for the dielectric response of nonmetallic crystals. Journal of Chemical Physics 112, 6517 (2000)
P. Romaniello and P.L. de Boeij, Time-dependent current-density-functional theory for the metallic response of solids. Physical Review B 71, 155108 (2005)
Main applications
F. Kootstra, P.L. de Boeij, and J.G. Snijders, Application of time-dependent density-functional theory to the dielectric function of various nonmetallic crystals. Physical Review B 62, 7071 (2000)
P. Romaniello, P.L. de Boeij, F. Carbone, and D. van der Marel, Optical properties of bcc transition metals in the range 0.40 eV. Physical Review B 73, 075115 (2006)
Suggested book references
F. Kootstra, Ph.D. thesis, Rijksuniversiteit Groningen, Groningen (2001).
P. Romaniello, Ph.D. thesis, Rijksuniversiteit Groningen, Groningen (2006).
A. Berger, Ph.D. thesis, Rijksuniversiteit Groningen, Groningen (2006).
P. Romaniello and P.L. de Boeij, Relativistic two-component formulation of time-dependent current-density functional theory: Application to the linear response of solids. Journal of Chemical Physics 127, 174111 (2007)
Lead
J.A. Berger, P.L. de Boeij and R. van Leeuwen, Analysis of the viscoelastic coefficients in the Vignale-Kohn functional: The cases of one- and three-dimensional polyacetylene. Physical Review B 71, 155104 (2005)
Applications
J.A. Berger, P. Romaniello, R. van Leeuwen and P.L. de Boeij, Performance of the Vignale-Kohn functional in the linear response of metals. Physical Review B 74, 245117 (2006)
J.A. Berger, P.L. de Boeij, and R. van Leeuwen, Analysis of the Vignale-Kohn current functional in the calculation of the optical spectra of semiconductors. Physical Review B 75, 35116 (2007)
Lead
D. Skachkov, M. Krykunov, E. Kadantsev, and T. Ziegler, The Calculation of NMR Chemical Shifts in Periodic Systems Based on Gauge Including Atomic Orbitals and Density Functional Theory. Journal of Chemical Theory and Computation 6, 1650 (2010)
D. Skachkov, M. Krykunov, and T. Ziegler, An improved scheme for the calculation of NMR chemical shifts in periodic systems based on gauge including atomic orbitals and density functional theory, Canadian Journal of Chemistry 89, 1150 (2011).
A-tensor: Nuclear magnetic dipole hyperfine interaction
E.S. Kadantsev and T. Ziegler, Implementation of a Density Functional Theory-Based Method for the Calculation of the Hyperfine A-tensor in Periodic Systems with the Use of Numerical and Slater Type Atomic Orbitals: Application to Paramagnetic Defects. Journal of Physical Chemistry A 112, 4521 (2008)
G-tensor: Zeeman interaction
E.S. Kadantsev and T. Ziegler, Implementation of a DFT Based Method for the Calculation of Zeeman g-tensor in Periodic Systems with the use of Numerical and Slater Type Atomic Orbitals. Journal of Physical Chemistry A 113, 1327 (2009)
When you publish results in the scientific literature that were obtained with one of the included force fields for ReaxFF, including the proper reference for the force field used is mandatory.
AB (Ammonia Borane):
M.R. Weismiller, A.C.T. van Duin, J. Lee, R.A. Yetter, ReaxFF Reactive Force Field Development and Applications for Molecular Dynamics Simulations of Ammonia Borane Dehydrogenation and Combustion. Journal of Physical Chemistry A 114, 5485-5492 (2010)
AuO:
J.A. Keith, D. Fantauzzi, T. Jacob, A.C.T. van Duin, Reactive forcefield for simulating gold surfaces and nanoparticles. Physical Review B 81, 235404 (2010)
CHO (Hydrocarbon oxidation):
K. Chenoweth, A.C.T. van Duin, W.A. Goddard, ReaxFF Reactive Force Field for Molecular Dynamics Simulations of Hydrocarbon Oxidation. Journal of Physical Chemistry A 112, 1040-1053 (2008)
HCONSB:
K. Chenoweth, A.C.T. van Duin, W.A. Goddard, ReaxFF Reactive Force Field for Molecular Dynamics Simulations of Hydrocarbon Oxidation. Journal of Physical Chemistry A 112, 1040-1053 (2008)
F. Castro-Marcano, A.M. Kamat, M.F. Russo, A.C.T. van Duin and J.P. Mathews, Combustion of an Illinois No. 6 Coal Char Simulated Using an Atomistic Char Representation and the ReaxFF Reactive Force Field. Combustion and Flame ASAP, (2011).
M.R. Weismiller, A.C.T. van Duin, J. Lee and R.A. Yetter, ReaxFF Reactive Force Field Development and Applications for Molecular Dynamics Simulations of Ammonia Borane Dehydrogenation and Combustion. Journal of Physical Chemistry A 114, 5485-5492 (2010).
F. Castro-Marcano, A. M. Kamat, M. F. Russo Jr., A. C. T. van Duin, J. P. Matthews, Combustion of an Illinois No. 6 coal char simulated using an atomistic char representation and the ReaxFF reactive force field Combustion and Flame, 159 (3), 1272-1285 (2012).
Cu-water:
A.C.T. van Duin, V.S. Bryantsev, M.S. Diallo, W.A. Goddard, O. Rahaman, D.J. Doren, D. Raymand, and K. Hermansson, Development and validation of a ReaxFF reactive force field for Cu cation/water interactions and copper metal/metal oxide/metal hydroxide condensed phases. Journal of Physical Chemistry A 114, 9507-9514 (2010)
FeOCH:
M. Aryanpour, A.C.T. van Duin, J.D. Kubicki, Article Development of a Reactive Force Field for Iron.Oxyhydroxide Systems. Journal of Physical Chemistry A 114, 6298-6307 (2010)
HE (RDX/High Energy):
A. Strachan, A.C.T. van Duin, D. Chakraborty, S. Dasgupta, W.A. Goddard III, Shock Waves in High-Energy Materials: The Initial Chemical Events in Nitramine RDX. Physical Review Letters 91, 098301 (2003)
A. Strachan, E. Kober, A.C.T. van Duin, J. Oxgaard, W.A. Goddard III, Thermal decomposition of RDX from reactive molecular dynamics. Journal of Chemical Physics 122, 054502 (2005)
L. Zhang, A.C.T. van Duin, S. Zybin, W.A. Goddard, Thermal Decomposition of Hydrazines from Reactive Dynamics Using the ReaxFF Reactive Force Field. Journal of Physical Chemistry B 113, 10770-10778 (2009)
L. Zhang, S. Zybin, A.C.T. van Duin, S. Dasgupta, W.A. Goddard, E.J. Kober, Carbon Cluster Formation during Thermal Decomposition of Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine and 1,3,5-Triamino-2,4,6-trinitrobenzene High Explosives from ReaxFF Reactive Molecular Dynamics Simulations. Journal of Physical Chemistry A 113, 10619-10640 (2009)
NaH:
J.G.O. Ojwang, R. Van Santen, G.J. Kramer, A.C.T. van Duin, and W.A. Goddard, Modeling the sorption dynamics of NaH using a reactive force field. Journal of Chemical Physics 128, 164714 (2008)
NiCH:
J.E. Mueller, A.C.T. van Duin, and W.A. Goddard, III, Development and Validation of ReaxFF Reactive Force Field for Hydrocarbon Chemistry Catalyzed by Nickel. Journal of Physical Chemistry C 114, 4939-4949 (2010)
SiOH:
Fogarty, J. C.; Aktulga, H. M.; Grama, A. Y.; van Duin, A. C. T. and Pandit, S. A., A reactive molecular dynamics simulation of the silica-water interface. J. Chem. Phys. 132, 174704 (2010)
VOCH:
K. Chenoweth, A.C.T. van Duin, P. Persson, M.J. Cheng, J. Oxgaard, W.A. Goddard, Development and Application of a ReaxFF Reactive Force Field for Oxidative Dehydrogenation on Vanadium Oxide Catalysts. Journal of Physical Chemistry C 112, 14645-14654 (2008)
ZnOH:
D. Raymand, A.C.T. van Duin, M. Baudin, K. Hermannson, A reactive force field (ReaxFF) for zinc oxide. Surface Science 602 (5), 1020-1031 (2008)
D. Raymand, A.C.T. van Duin, D. Spangberg, W.A. Goddard, K. Hermansson, Water adsorption on stepped ZnO surfaces from MD simulation. Surface Science 604 (9-10), 741-752 (2010)
When you publish results in the scientific literature that were obtained with one of the included parameter sets for DFTB, including the proper reference for the force field used is mandatory.
mio-0-1 from DFTB.org
For systems containing O, N, C, H:
M. Elstner, D. Porezag, G. Jungnickel, J. Elstner, M. Haugk, Th. Frauenheim, S. Suhai, G. Seifert,
Self-consistent-charge density-functional tight-binding method for simulations of complex materials properties.
Phys. Rev. B 58, 7260-7268 (1998)
For systems also containing S:
T. A. Niehaus, M. Elstner, Th. Frauenheim, S. Suhai,
Application of an approximate density-functional method to sulfur containing compounds.
J. Mol. Struc. (THEOCHEM) 541, 185-194 (2001)
mio-1-1 from DFTB.org
For systems containing O, N, C, H:
M. Elstner, D. Porezag, G. Jungnickel, J. Elstner, M. Haugk, Th. Frauenheim, S. Suhai, G. Seifert,
Self-consistent-charge density-functional tight-binding method for simulations of complex materials properties.
Phys. Rev. B 58, 7260-7268 (1998)
For systems also containing S:
T. A. Niehaus, M. Elstner, Th. Frauenheim, S. Suhai,
Application of an approximate density-functional method to sulfur containing compounds.
J. Mol. Struc. (THEOCHEM) 541, 185-194 (2001)
For systems also containing P:
M. Gaus, Q. Cui, M. Elstner,
DFTB3: Extension of the Self-Consistent-Charge Density-Functional Tight-Binding Method (SCC-DFTB)
J. Chem. Theory Comput. 7, 931-948 (2011)
chalc-0-1 from DFTB.org
Include the DFTB.org/mio-0-1 references and add for As-S-H containing systems the chalc_0_1 reference:
S.I. Simdyankin, S.R. Elliott, T.A. Niehaus, and T. Frauenheim, in Computational Modeling and Simulation of Materials III, vol. A. P. Vincenzini, A. Lami, F. Zerbetto,Eds.; Techna Group s.r.l., Faenza, Italy, 2004, pp. 149
matsci-0-3 from DFTB.org
The complete set:
J. Frenzel, A. F. Oliveira, N. Jardillier, T. Heine, G. Seifert,
Semi-relativistic, self-consistent charge Slater-Koster tables for density-functional based tight-binding (DFTB) for materials science simulations. TU-Dresden 2004-2009
For systems containing Al, O, and H:
J. Frenzel, A. F. Oliveira, H. A. Duarte, T. Heine, G. Seifert,
Structural and electronic properties of bulk gibbsite and gibbsite surfaces. Z. Anorg. Allg. Chem. 631, 1267-1271 (2005)
For systems containing Al, Si, O, and H:
L. Guimaraes, A. N. Enyashin, J. Frenzel, T. Heine, H. A. Duarte, G. Seifert,
Imogolite Nanotubes: Stability, electronic and mechanical properties. Nano 1, 362-368 (2007)
For systems containing Al, O, P, C, and H:
R. Luschtinetz, A. F. Oliveira, J. Frenzel, J. Joswig, G. Seifert, H. A. Duarte,
Adsorption of phosphonic and ethylphosphonic acid on aluminum oxide surfaces. Surf. Sci. 602, 1347-1359 (2008)
For systems containing Ti, O, P, C, and H:
R. Luschtinetz, J. Frenzel, T. Milek, G. Seifert
Adsorption of phosphonic acid at the TiO2 anatase (101) and rutile (110) surface. J. Phys. Chem. C 113, 5730-5740 (2009)
For systems containing Ti, N, O, P, C, and H:
A. Enyashin, J. Frenzel, S. Gemming, G. Seifert
Adsorption of nucleotides on the rutile (110) surface. Int. J. Mat. Res. 101, 768-764 (2010)
For systems containing Cu-Si, Cu-O, Cu-H, Cu-Na, Na-H, Na-Si, Na-O:
N. Jardillier, Ph.D. Thesis , Universite Montpellier II, Montpellier (2006)
miomod-hh-0-1 from DFTB.org
Modification of the DFTB.org/mio parameters for H-H potentials. Use appropriate mio references.
miomod-hn-0-1 from DFTB.org
Modification of the DFTB.org/mio parameters for N-H potentials. Use appropriate mio references and add for N-H:
A. Bondar, S. Fischer, J. C. Smith, M. Elstner, S. Suhai, Key Role of Electrostatic Interactions in Bacteriorhodopsin Proton Transfer. J. Am. Chem. Soc. 126, 14668-14677 (2004)
pbc-0-3 from DFTB.org
For systems containing Si:
A. Sieck, Ph.D. Thesis, University of Paderborn, Paderborn (2000).
For systems containing Si and C:
E. Rauls, R. Gutierrez, J. Elsner, Th. Frauenheim,
Stoichiometric and non-stoichiometric (1010) and (1120) surfaces in 2H-SiC: a theoretical study. Sol. State Comm. 111, 459-464 (1999)
For systems containing Si and O:
C. Koehler, Z. Hajnal, P. Deak, Th. Frauenheim, S. Suhai,
Theoretical investigation of carbon defects and diffusion in alpha-quartz. Phys. Rev. B 64, 085333 (2001)
For systems containing F (and Si, O, N, C, H):
C. Koehler, Th. Frauenheim,
Molecular dynamics simulations of CFx (x = 2, 3) molecules at Si3N4 and SiO2 surfaces. Surf. Sci. 600, 453-460 (2003)
For systems containing F (and Si, O, N, C, H):
C. Koehler, G. Seifert, Th. Frauenheim
Density functional based calculations for Fe_n (n ≤ 32). Chem. Phys. 309, 23-31 (2005)
tiorg-0-1 from DFTB.org
In addition to the mio set, cite:
G. Dolgonos, B. Aradi, N. H. Moreira, T. Frauenheim,
An Improved Self-Consistent-Charge Density-Functional Tight-Binding (SCC-DFTB) Set of Parameters for Simulation of Bulk and Molecular Systems Involving Titanium.
J. Chem. Theory Compt. 6, 266-278 (2010)
trans3d-0-1 from DFTB.org
In addition to the mio set, cite:
G. Zheng, H. A. Witek, P. Bobadova-Parvanova, S. Irle, D. G. Musaev, R. Prabhakar, K. Morokuma, M. Lundberg, M. Elstner, C. Kohler, T. Frauenheim,
Parameter Calibration of Transition-Metal Elements for the Spin-Polarized Self-Consistent-Charge Density-Functional Tight-Binding (DFTB) Method: Sc, Ti, Fe, Co, and Ni.
J. Chem. Theory Compt. 4, 1349-1367 (2007)
znorg-0-1 from DFTB.org
In addition to the mio set, cite:
N.H. Moreira, G. Dolgonos, B. Aradi, A. L. da Rosa, Th. Frauenheim,
Toward an Accurate Density-Functional Tight-Binding Description of Zinc-Containing Compounds.
J. Chem. Theory Compt. 4, 605-614 (2009)
Dresden
J. Frenzel, A. F. Oliveira, N. Jardillier, T. Heine, G. Seifert, Semi-relativistic, self-consistent charge Slater-Koster tables for density-functional based tight-binding (DFTB) for materials science simulations. TU-Dresden 2004-2009
J. Frenzel, A. F. Oliveira, H. A. Duarte, T. Heine, G. Seifert, Structural and electronic properties of bulk gibbsite and gibbsite surfaces. Z. Anorg. Allg. Chem. 631, 1267-1271 (2005)
L. Guimaraes, A. N. Enyashin, J. Frenzel, T. Heine, H. A. Duarte, G. Seifert, Imogolite Nanotubes: Stability, electronic and mechanical properties. Nano 1, 362-368 (2007)
R. Luschtinetz, A. F. Oliveira, J. Frenzel, J. Joswig, G. Seifert, H. A. Duarte, Adsorption of phosphonic and ethylphosphonic acid on aluminum oxide surfaces. Surf. Sci. 602, 1347-1359 (2008)
R. Luschtinetz, J. Frenzel, T. Milek, G. Seifert Adsorption of phosphonic acid at the TiO2 anatase (101) and rutile (110) surface. J. Phys. Chem. C 113, 5730-5740 (2009)
ThirdOrder
M. Elstner, D. Porezag, G. Jungnickel, J. Elstner, M. Haugk, Th. Frauenheim, S. Suhai, G. Seifert, Self-consistent-charge density-functional tight-binding method for simulations of complex materials properties. Phys. Rev. B 58, 7260-7268 (1998)
T. A. Niehaus, M. Elstner, Th. Frauenheim, S. Suhai, Application of an approximate density-functional method to sulfur containing compounds. J. Mol. Struc. (THEOCHEM) 541, 185-194 (2001)
M. Gaus, Q. Cui, M. Elstner, DFTB3: Extension of the Self-Consistent-Charge Density-Functional Tight-Binding Method (SCC-DFTB). J. Chem. Theory Comput. 7, 931-948 (2011)
The next programs and/or libraries are used in the ADF package. On some platforms optimized libraries have been used and/or vendor specific MPI implementations.
Description:
the scripting language used internally within the ADF package
Site:
License:
BSD-style open source license
This software is copyrighted by the Regents of the University of California, Sun Microsystems, Inc., Scriptics Corporation, ActiveState Corporation and other parties. The following terms apply to all files associated with the software unless explicitly disclaimed in individual files. The authors hereby grant permission to use, copy, modify, distribute, and license this software and its documentation for any purpose, provided that existing copyright notices are retained in all copies and that this notice is included verbatim in any distributions. No written agreement, license, or royalty fee is required for any of the authorized uses. Modifications to this software may be copyrighted by their authors and need not follow the licensing terms described here, provided that the new terms are clearly indicated on the first page of each file where they apply. IN NO EVENT SHALL THE AUTHORS OR DISTRIBUTORS BE LIABLE TO ANY PARTY FOR DIRECT, INDIRECT, SPECIAL, INCIDENTAL, OR CONSEQUENTIAL DAMAGES ARISING OUT OF THE USE OF THIS SOFTWARE, ITS DOCUMENTATION, OR ANY DERIVATIVES THEREOF, EVEN IF THE AUTHORS HAVE BEEN ADVISED OF THE POSSIBILITY OF SUCH DAMAGE. THE AUTHORS AND DISTRIBUTORS SPECIFICALLY DISCLAIM ANY WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, AND NON-INFRINGEMENT. THIS SOFTWARE IS PROVIDED ON AN "AS IS" BASIS, AND THE AUTHORS AND DISTRIBUTORS HAVE NO OBLIGATION TO PROVIDE MAINTENANCE, SUPPORT, UPDATES, ENHANCEMENTS, OR MODIFICATIONS. GOVERNMENT USE: If you are acquiring this software on behalf of the U.S. government, the Government shall have only "Restricted Rights" in the software and related documentation as defined in the Federal Acquisition Regulations (FARs) in Clause 52.227.19 (c) (2). If you are acquiring the software on behalf of the Department of Defense, the software shall be classified as "Commercial Computer Software" and the Government shall have only "Restricted Rights" as defined in Clause 252.227-7013 (b) (3) of DFARs. Notwithstanding the foregoing, the authors grant the U.S. Government and others acting in its behalf permission to use and distribute the software in accordance with the terms specified in this license.
Description:
standard library belonging to Tcl/Tk
Site:
http://www.tcl.tk/software/tcllib/
License:
BSD
On the TclTk wiki the following is mentioned about the license:
In response to popular demand, the Tcl core group is introducing tcllib, a Tcl standard library. This meta-package will contain many modules, each of which is itself a standalone Tcl package. The intention is to provide commonly used functions and libraries, bundled together under a single license (BSD), and with no binary dependencies.
The following text is included with both the tcllib and tklib distributions in license.terms:
This software is copyrighted by Ajuba Solutions and other parties. The following terms apply to all files associated with the software unless explicitly disclaimed in individual files. The authors hereby grant permission to use, copy, modify, distribute, and license this software and its documentation for any purpose, provided that existing copyright notices are retained in all copies and that this notice is included verbatim in any distributions. No written agreement, license, or royalty fee is required for any of the authorized uses. Modifications to this software may be copyrighted by their authors and need not follow the licensing terms described here, provided that the new terms are clearly indicated on the first page of each file where they apply. IN NO EVENT SHALL THE AUTHORS OR DISTRIBUTORS BE LIABLE TO ANY PARTY FOR DIRECT, INDIRECT, SPECIAL, INCIDENTAL, OR CONSEQUENTIAL DAMAGES ARISING OUT OF THE USE OF THIS SOFTWARE, ITS DOCUMENTATION, OR ANY DERIVATIVES THEREOF, EVEN IF THE AUTHORS HAVE BEEN ADVISED OF THE POSSIBILITY OF SUCH DAMAGE. THE AUTHORS AND DISTRIBUTORS SPECIFICALLY DISCLAIM ANY WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, AND NON-INFRINGEMENT. THIS SOFTWARE IS PROVIDED ON AN "AS IS" BASIS, AND THE AUTHORS AND DISTRIBUTORS HAVE NO OBLIGATION TO PROVIDE MAINTENANCE, SUPPORT, UPDATES, ENHANCEMENTS, OR MODIFICATIONS. GOVERNMENT USE: If you are acquiring this software on behalf of the U.S. government, the Government shall have only "Restricted Rights" in the software and related documentation as defined in the Federal Acquisition Regulations (FARs) in Clause 52.227.19 (c) (2). If you are acquiring the software on behalf of the Department of Defense, the software shall be classified as "Commercial Computer Software" and the Government shall have only "Restricted Rights" as defined in Clause 252.227-7013 (c) (1) of DFARs. Notwithstanding the foregoing, the authors grant the U.S. Government and others acting in its behalf permission to use and distribute the software in accordance with the terms specified in this license.
Description:
the visualization toolkit used by the GUI
Site:
License:
BSD license
VTK is an open-source toolkit licensed under the BSD license.
Copyright (c) 1993-2008 Ken Martin, Will Schroeder, Bill Lorensen
All rights reserved.
Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions are met:
THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS ``AS IS'' AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE AUTHORS OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Description:
Linear Algebra library
Site:
License:
unknown
The following information is from the BLAS FAQ on the mentioned site:
2) Are there legal restrictions on the use of BLAS reference implementation software?The reference BLAS is a freely-available software package. It is available from netlib via anonymous ftp and the World Wide Web. Thus, it can be included in commercial software packages (and has been). We only ask that proper credit be given to the authors.
Like all software, it is copyrighted. It is not trademarked, but we do ask the following:
If you modify the source for these routines we ask that you change the name of the routine and comment the changes made to the original.
We will gladly answer any questions regarding the software. If a modification is done, however, it is the responsibility of the person who modified the routine to provide support.
Description:
Linear Algebra library
Site:
License:
modified BSD
Copyright (c) 1992-2010 The University of Tennessee and The University
of Tennessee Research Foundation. All rights
reserved.
Copyright (c) 2000-2010 The University of California Berkeley. All
rights reserved.
Copyright (c) 2006-2010 The University of Colorado Denver. All rights
reserved.
$COPYRIGHT$
Additional copyrights may follow
$HEADER$
Redistribution and use in source and binary forms, with or without
modification, are permitted provided that the following conditions are
met:
- Redistributions of source code must retain the above copyright
notice, this list of conditions and the following disclaimer.
- Redistributions in binary form must reproduce the above copyright
notice, this list of conditions and the following disclaimer listed
in this license in the documentation and/or other materials
provided with the distribution.
- Neither the name of the copyright holders nor the names of its
contributors may be used to endorse or promote products derived from
this software without specific prior written permission.
The copyright holders provide no reassurances that the source code
provided does not infringe any patent, copyright, or any other
intellectual property rights of third parties. The copyright holders
disclaim any liability to any recipient for claims brought against
recipient by any third party for infringement of that parties
intellectual property rights.
THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS
"AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT
LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR
A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT
OWNER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL,
SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT
LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE,
DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY
THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT
(INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE
OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Description:
implementation of a subset of LAPACK routines for parallel computers
Site:
http://www.netlib.org/scalapack/
License:
modified BSD
Copyright (c) 1992-2009 The University of Tennessee. All rights reserved. $COPYRIGHT$ Additional copyrights may follow $HEADER$ Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions are met: - Redistributions of source code must retain the above copyright notice, this list of conditions and the following disclaimer. - Redistributions in binary form must reproduce the above copyright notice, this list of conditions and the following disclaimer listed in this license in the documentation and/or other materials provided with the distribution. - Neither the name of the copyright holders nor the names of its contributors may be used to endorse or promote products derived from this software without specific prior written permission. THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT OWNER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Description:
scripting language
Site:
License:
open source, GPL compatible
Click to read the license conditions printed by Python 2.6 by using the license() function.
Description:
Libary for scientific computing with Python
Site:
License:
BSD License
Numpy license Copyright © 2005-2010, NumPy Developers. All rights reserved. Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions are met: Redistributions of source code must retain the above copyright notice, this list of conditions and the following disclaimer. Redistributions in binary form must reproduce the above copyright notice, this list of conditions and the following disclaimer in the documentation and/or other materials provided with the distribution. Neither the name of the NumPy Developers nor the names of any contributors may be used to endorse or promote products derived from this software without specific prior written permission. THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS “AS IS” AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT OWNER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Description:
Open source MPI-2 implementation
Site:
License:
New BSD License
Following is the text of the New BSD license, taken from http://www.open-mpi.org/community/license.php:
Most files in this release are marked with the copyrights of the
organizations who have edited them. The copyrights below are in no
particular order and generally reflect members of the Open MPI core
team who have contributed code to this release. The copyrights for
code used under license from other parties are included in the
corresponding files.
Copyright (c) 2004-2010 The Trustees of Indiana University and Indiana
University Research and Technology
Corporation. All rights reserved.
Copyright (c) 2004-2010 The University of Tennessee and The University
of Tennessee Research Foundation. All rights
reserved.
Copyright (c) 2004-2010 High Performance Computing Center Stuttgart,
University of Stuttgart. All rights reserved.
Copyright (c) 2004-2008 The Regents of the University of California.
All rights reserved.
Copyright (c) 2006-2010 Los Alamos National Security, LLC. All rights
reserved.
Copyright (c) 2006-2010 Cisco Systems, Inc. All rights reserved.
Copyright (c) 2006-2010 Voltaire, Inc. All rights reserved.
Copyright (c) 2006-2010 Sandia National Laboratories. All rights reserved.
Copyright (c) 2006-2010 Sun Microsystems, Inc. All rights reserved.
Use is subject to license terms.
Copyright (c) 2006-2010 The University of Houston. All rights reserved.
Copyright (c) 2006-2009 Myricom, Inc. All rights reserved.
Copyright (c) 2007-2008 UT-Battelle, LLC. All rights reserved.
Copyright (c) 2007-2010 IBM Corporation. All rights reserved.
Copyright (c) 1998-2005 Forschungszentrum Juelich, Juelich Supercomputing
Centre, Federal Republic of Germany
Copyright (c) 2005-2008 ZIH, TU Dresden, Federal Republic of Germany
Copyright (c) 2007 Evergrid, Inc. All rights reserved.
Copyright (c) 2008 Chelsio, Inc. All rights reserved.
Copyright (c) 2008-2009 Institut National de Recherche en
Informatique. All rights reserved.
Copyright (c) 2007 Lawrence Livermore National Security, LLC.
All rights reserved.
Copyright (c) 2007-2009 Mellanox Technologies. All rights reserved.
Copyright (c) 2006-2010 QLogic Corporation. All rights reserved.
Copyright (c) 2008-2010 Oak Ridge National Labs. All rights reserved.
Copyright (c) 2006-2010 Oracle and/or its affiliates. All rights reserved.
Copyright (c) 2009 Bull SAS. All rights reserved.
Copyright (c) 2010 ARM ltd. All rights reserved.
$COPYRIGHT$
Additional copyrights may follow
$HEADER$
Redistribution and use in source and binary forms, with or without
modification, are permitted provided that the following conditions are
met:
- Redistributions of source code must retain the above copyright
notice, this list of conditions and the following disclaimer.
- Redistributions in binary form must reproduce the above copyright
notice, this list of conditions and the following disclaimer listed
in this license in the documentation and/or other materials
provided with the distribution.
- Neither the name of the copyright holders nor the names of its
contributors may be used to endorse or promote products derived from
this software without specific prior written permission.
The copyright holders provide no reassurances that the source code
provided does not infringe any patent, copyright, or any other
intellectual property rights of third parties. The copyright holders
disclaim any liability to any recipient for claims brought against
recipient by any third party for infringement of that parties
intellectual property rights.
THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS
"AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT
LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR
A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT
OWNER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL,
SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT
LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE,
DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY
THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT
(INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE
OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Description:
High performance MPI implementation (formerly HP-MPI)
Site:
http://www.platform.com/Products/platform-mpi
License:
Commercial
Description:
The Open Source Chemistry Toolbox
OpenBabel is used as an external command to convert input formats.
Site:
License:
GNU General Public License GPL2
Click to read the COPYING file as included with OpenBabel (the GPL2 license).
Description:
Atomistic Simulation Environment
ASE is used to perform MD simulations within pymd.
Site:
https://wiki.fysik.dtu.dk/ase/overview.html
Reference:
If you find ASE useful in your research please cite:
S. R. Bahn and K. W. Jacobsen An object-oriented scripting interface to a legacy electronic structure code Comput. Sci. Eng., Vol. 4, 56-66, 2002
License:
GNU Lesser General Public License version 2.1
LICENSE included in the distribution:
ASE is free software: you can redistribute it and/or modify it under the terms of the GNU Lesser General Public License as published by the Free Software Foundation, either version 2.1 of the License, or (at your option) any later version. ASE is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU Lesser General Public License for more details. You should have received a copy of the GNU Lesser General Public License along with ASE. If not, see http://www.gnu.org/licenses/.
Description:
PLUMED is an open source plugin for free energy calculations in molecular systems.
Site:
Reference:
You may wish to cite the following reference if you have utilized PLUMED in your work:
Bonomi, D. Branduardi, G. Bussi, C. Camilloni, D. Provasi, P. Raiteri, D. Donadio, F. Marinelli, F. Pietrucci, R.A. Broglia and M. Parrinello PLUMED: a portable plugin for free-energy calculations with molecular dynamics, Comp. Phys. Comm. 2009 vol. 180 (10) pp. 1961-1972.
License:
GNU Lesser General Public License version 3
LICENSE included in the distribution:
PLUMED is free software: you can redistribute it and/or modify it under the terms of the GNU Lesser General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. PLUMED is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU Lesser General Public License for more detail. You should have received a copy of the GNU Lesser General Public License along with PLUMED. If not, see http://www.gnu.org/licenses/.
Description:
Packing Optimization for Molecular Dynamics Simulations
Packmol (version of november 2009) is used to generate MD starting geometries. No changes have been made to the source code, and the version of the source code that we have used is included in $ADFHOME/Install/packmol.tar (november 2009).
Packmol is executed as an (external) stand-alone command via the GUI.
Site:
http://www.ime.unicamp.br/~martinez/packmol/
License:
GPL 3
Click to read the COPYING file as included with Packmol (the GPL3 license).
Following is the AUTHORS file as included with Packmol: ======================================================= L. Martinez, R. Andrade, E. G. Birgin, J. M. Martinez, Packmol: A package for building initial configurations for molecular dynamics simulations. Journal of Computational Chemistry, 30 (13): 2157-2164 (2009). J. M. Martinez and L. Martinez, Packing optimization for automated generation of complex system's initial configurations for molecular dynamics and docking. Journal of Computational Chemistry, 24 (7): 819-825 (2003). Home-Page: http://www.ime.unicamp.br/~martinez/packmol
Description:
Program to find symmetry of a molecule
Reference:
Symmol: T. Pilati and A. Forni, SYMMOL: a program to find the maximum symmetry group in an atom cluster, given a prefixed tolerance, Journal of Applied Crystallography 31, 503 (1998)
Description:
Macroscopic Electrostatics with Atomic Detail
Site:
http://www.stjuderesearch.org/bashford-mead
Description:
Open source text-indexing tool
Starting with the 2011 release, Swish-e will be included and is used as an external program to search the documentation.
Site:
License:
a modified version of GNU GPL2
Click to read the full license (taken from http://swish-e.org/license.html).
Description:
Library to compute the discrete Fourier transform
Site:
License:
commercial
Description:
XCFun is a library of approximate exchange-correlation functionals
Site:
License:
A modified LGPL license that allows SCM to link statically with XCFun
The XCFun library is licensed under the LGPL license. This means that you may modify and distribute the library freely as long as you also release any changes made by you under the LGPL license. If you are just making modifications without distributing the modified library you are not obliged to release your changes. However, we do of course welcome all contributions as long as they are well tested and thought out
Reference:
Ulf Ekström, Lucas Visscher, Radovan Bast, Andreas J. Thorvaldsen and Kenneth Ruud,
Arbitrary-Order Density Functional Response Theory from Automatic Differentiation,
Journal of Chemical Theory and Computation 6, 1971 (2010), DOI: 10.1021/ct100117s
Description:
A version of the X.Org X Window System that runs on OS X
The Mac OS X version (64 bit) uses XQuartz to run on Mountain Lion. The ADF2012.01.app aplication is a modified XQuartz.app, retaining the original copyright messages. The change is that after starting the Xserver the ADF-GUI application is automatically started.
Site:
License:
An XQuartz installation consists of many individual pieces of software which have various licenses. The X.Org software components’ licenses are discussed on the X.Org Foundation Licenses page. The quartz-wm window manager included with the XQuartz distribution uses the Apple Public Source License Version 2.
