Open AccessFurther investigations of linear trirhodium complexes: experimental and theoretical studies of [Rh3(dpa)4Cl2] and [Rh3(dpa)4Cl2](BF4) [dpa = bis(2-pyridyl)amido anion]
Author(s) -
GinChen Huang,
Isiah PoChun Liu,
JauHuei Kuo,
YiLin Huang,
ChenYu Yeh,
GeneHsiang Lee,
ShieMing Peng
Publication year - 2009
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/b820060b
Subject(s) - unpaired electron , chemistry , spin crossover , singlet state , atomic orbital , spin states , molecular orbital , computational chemistry , crystallography , electron , inorganic chemistry , molecule , atomic physics , excited state , organic chemistry , physics , quantum mechanics
The linear trirhodium compound, Rh3(dpa)4Cl2 (1), and its one-electron oxidation product, [Rh3(dpa)4Cl2]BF4 (2), have been synthesized and studied extensively. The magnetic measurement for compound 1 shows that it possesses one unpaired electron that is assigned to occupy the sigma(nb) orbital (2A2) by DFT calculations. Upon oxidation, a beta-spin electron of 1 is removed, that causes compound 2 to exhibit a triplet ground state. DFT calculations indicate that the two unpaired electrons of 2 occupy sigma(nb) and delta* orbitals (3B1), which is supported by 1H NMR spectrum. Unlike their isoelectronic analogues [Co3(dpa)4Cl2] (3) and [Co3(dpa)4(Cl)2]BF4 (4), both compound 1 and 2 do not display the spin-crossover phenomenon. The reason may be attributed to the relative large energy gap between 3B1 and open-shell singlet 1B1 states.
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