Aspects of intervalence charge transfer in cyanide-bridged systems: Modulated electric field assessment of distances, polarizability changes, and anticipated first hyperpolarizability characteristics

被引:42
作者
Vance, FW
Karki, L
Reigle, JK
Hupp, JT
Ratner, MA
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Mat Res, Evanston, IL 60208 USA
关键词
D O I
10.1021/jp981352j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electroabsorption studies of the systems (CN)(5)M-II-CN-M'(III)(NH3)(5)(1-) (M = Fe, Ru, Os; M' = Ru, Os) reveal that the metal-to-metal or intervalence charge-transfer transitions are associated with a change in dipole moment, \Delta mu\, ranging from 11 to 17 D. This change corresponds to a charge-transfer distance of ca. one-half to two-thirds of the geometric separation between the donor and acceptor metals. This result has consequences for electron transfer parameters, where electronic coupling energies are now upwardly revised to as high as 3000 cm(-1). The result is also pertinent in the context of nonlinear optics, where Delta mu can be utilized in a two level model to estimate wavelength-dependent molecular first hyperpolarizabilities. The change in polarizability (Delta alpha) accompanying the optical intervalence transitions varies from -10 to +310 Angstrom(3). Comparing the experimental results to a simple two state model suggests that the two state picture is seriously deficient for these systems and that a multitude of available additional states must be included to achieve a quantitative description of the polarizable intervalence excited states of these systems.
引用
收藏
页码:8320 / 8324
页数:5
相关论文
共 30 条
[1]   Geometric structure and second-order nonlinear optical response of substituted calix[4]arene molecules: A theoretical study [J].
Brouyere, E ;
Persoons, A ;
Bredas, JL .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (22) :4142-4148
[2]  
BUBLITZ, 1998, IN PRESS J AM CHEM S
[3]   Stark spectroscopy: Applications in chemistry, biology, and materials science [J].
Bublitz, GU ;
Boxer, SG .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1997, 48 :213-242
[4]   Generalization of the Mulliken-Hush treatment for the calculation of electron transfer matrix elements [J].
Cave, RJ ;
Newton, MD .
CHEMICAL PHYSICS LETTERS, 1996, 249 (1-2) :15-19
[5]   METAL-LIGAND AND METAL-METAL COUPLING ELEMENTS [J].
CREUTZ, C ;
NEWTON, MD ;
SUTIN, N .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1994, 82 (1-3) :47-59
[6]  
DENNING RG, 1993, ADV SPECTROSC, P1
[7]   Large second-order optical nonlinearities in open-shell chromophores. Planar metal complexes and organic radical ion aggregates [J].
DiBella, S ;
Fragala, I ;
Marks, TJ ;
Ratner, MA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (50) :12747-12751
[8]   PROPERTIES OF THE MIXED-VALENCE BINUCLEAR COMPLEX ION, [(NH3)5RUIII-NC-OSII(CN)5] [J].
FORLANO, P ;
BARALDO, LM ;
OLABE, JA ;
DELLAVEDOVA, CO .
INORGANICA CHIMICA ACTA, 1994, 223 (1-2) :37-42
[9]   DESIGN AND CONSTRUCTION OF MOLECULAR ASSEMBLIES WITH LARGE 2ND-ORDER OPTICAL NONLINEARITIES - QUANTUM-CHEMICAL ASPECTS [J].
KANIS, DR ;
RATNER, MA ;
MARKS, TJ .
CHEMICAL REVIEWS, 1994, 94 (01) :195-242
[10]   Electroabsorption studies of intervalence charge transfer in (NC)(5)FeCNOs(NH3)(5)(-): Experimental assessment of charge-transfer distance, solvent reorganization, and electronic coupling parameters [J].
Karki, L ;
Lu, HP ;
Hupp, JT .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (39) :15637-15639