Large Changes of Static Electric Properties Induced by Hydrogen Bonding: An ab Initio Study of Linear HCN Oligomers


Autoria(s): GORA, Robert W.; ZALESNY, Robert; ZAWADA, Agnieszka; BARTKOWIAK, Wojciech; SKWARA, Bartlomiej; PAPADOPOULOS, Manthos G.; SILVA, Daniel L.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

We report the partitioning of the interaction-induced static electronic dipole (hyper)polarizabilities for linear hydrogen cyanide complexes into contributions arising from various interaction energy terms. We analyzed the nonadditivities of the studied properties and used these data to predict the electric properties of an infinite chain. The interaction-induced static electric dipole properties and their nonadditivities were analyzed using an approach based on numerical differentiation of the interaction energy components estimated in an external electric field. These were obtained using the hybrid variational-perturbational interaction energy decomposition scheme, augmented with coupled-cluster calculations, with singles, doubles, and noniterative triples. Our results indicate that the interaction-induced dipole moments and polarizabilities are primarily electrostatic in nature; however, the composition of the interaction hyperpolarizabilities is much more complex. The overlap effects substantially quench the contributions due to electrostatic interactions, and therefore, the major components are due to the induction and exchange induction terms, as well as the intramolecular electron-correlation corrections. A particularly intriguing observation is that the interaction first hyperpolarizability in the studied systems not only is much larger than the corresponding sum of monomer properties, but also has the opposite sign. We show that this effect can be viewed as a direct consequence of hydrogen-bonding interactions that lead to a decrease of the hyperpolarizability of the proton acceptor and an increase of the hyperpolarizability of the proton donor. In the case of the first hyperpolarizability, we also observed the largest nonadditivity of interaction properties (nearly 17%) which further enhances the effects of pairwise interactions.

Wroclaw Center for Networking and Supercomputing (WCSS)

Wroclaw Center for Networking and Supercomputing (WCSS)

European Union

European Union

Iceland, Liechtenstein, and Norway through the EEA Financial Mechanism Scholarship and Training Fund

Iceland, Liechtenstein, and Norway through the EEA Financial Mechanism Scholarship and Training Fund

European Commission

European Commission[MRTN-CT-2006-035859]

Identificador

JOURNAL OF PHYSICAL CHEMISTRY A, v.115, n.18, p.4691-4700, 2011

1089-5639

http://producao.usp.br/handle/BDPI/29538

10.1021/jp110226h

http://dx.doi.org/10.1021/jp110226h

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Journal of Physical Chemistry A

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #NONLINEAR-OPTICAL-PROPERTIES #CORRELATED MOLECULAR CALCULATIONS #GAUSSIAN-BASIS SETS #CENTER-DOT-HE #INTERACTION ENERGY #1ST HYPERPOLARIZABILITY #PERTURBATION-THEORY #(HCN)(N) CLUSTERS #INTERMOLECULAR INTERACTIONS #2ND HYPERPOLARIZABILITIES #Chemistry, Physical #Physics, Atomic, Molecular & Chemical
Tipo

article

original article

publishedVersion