%0 Journal Article
%A Pan, Qing-Jiang
%A Zhang, Hong-Xing
%D 2004
%T Ab Initio Studies on Metal−Metal Interaction and 3[σ*(d)σ(s)] Excited State of the
Binuclear Au(I) Complexes Formed by Phosphine and/or Thioether Ligands
%U https://acs.figshare.com/articles/journal_contribution/Ab_Initio_Studies_on_Metal_Metal_Interaction_and_sup_3_sup_d_s_Excited_State_of_the_Binuclear_Au_I_Complexes_Formed_by_Phosphine_and_or_Thioether_Ligands/3341995
%R 10.1021/jp049873w.s001
%2 https://ndownloader.figshare.com/files/5181208
%K MP 2 level
%K substituent effect
%K CIS results
%K 2 species
%K MP 2 calculations
%K SCH
%K methyl groups
%K Ab Initio Studies
%K gas phase
%K MP 2
%K gold atom
%K CIS methods
%K emissive energy
%K PH 2 CH 2 SH
%K ground state
%K PH 2 CH 2 PH 2
%K optimized geometry
%K SHCH 2 SH
%K energy triplet
%K frequency calculations
%X The structures of ground state and lowest energy triplet excited state for [Au2(PH2CH2PH2)2]2+ (1), [Au2(PH2CH2PH2)(SHCH2SH)]2+ (2) and [Au2(SHCH2SH)2]2+ (3) as well as their solvated 1−3·(MeCN)2 species are
fully optimized by the MP2 and CIS methods, respectively. The 3[σ*(d)σ(s)] excited states give the 300−390
emissions in the gas phase, red shifting to 500−730 nm in acetonitrile. The coordination of solvent molecule
to the gold atom in the excited states is responsible for such a red shift. For 2, all the possible geometries, the
substituent effect of methyl groups on P and/or S atoms and the comparison with thiolate complex [Au2(PH2CH2PH2)(SCH2S)] (6) are discussed. The unrestricted MP2 calculations on 1−3, head-to-tail [Au2(PH2CH2SH)2]2+ (7) and head-to-head [Au2(PH2CH2SH)2]2+ (8) confirm the CIS results in both optimized geometry
and emissive energy related to the 3[σ*(d)σ(s)] state. The frequency calculations at the MP2 level indicate
that the Au(I)−Au(I) interaction is weak in the ground state (ν(Au2) = 89−101 cm-1) but is strongly
strengthened in the excited state (ν(Au2) = 144−189 cm-1).
%I ACS Publications