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Investigation of challenging spin systems using M onte C arlo configuration interaction and the density matrix renormalization group
Author(s) -
Coe Jeremy P.,
Almeida Nuno M. S.,
Paterson Martin J.
Publication year - 2017
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.25057
Subject(s) - physics , density matrix renormalization group , renormalization group , group (periodic table) , matrix (chemical analysis) , chemistry , mathematical physics , quantum mechanics , chromatography
We investigate if a range of challenging spin systems can be described sufficiently well using Monte Carlo configuration interaction (MCCI) and the density matrix renormalization group (DMRG) in a way that heads toward a more “black box” approach. Experimental results and other computational methods are used for comparison. The gap between the lowest doublet and quartet state of methylidyne (CH) is first considered. We then look at a range of first‐row transition metal monocarbonyls: MCO when M is titanium, vanadium, chromium, or manganese. For these MCO systems we also employ partially spin restricted open‐shell coupled‐cluster (RCCSD). We finally investigate the high‐spin low‐lying states of the iron dimer, its cation and its anion. The multireference character of these molecules is also considered. We find that these systems can be computationally challenging with close low‐lying states and often multireference character. For this more straightforward application and for the basis sets considered, we generally find qualitative agreement between DMRG and MCCI. © 2017 Wiley Periodicals, Inc.