Quantum Interference in Mixed-Valence Complexes: Tuning Electronic Coupling Through Substituent Effects.
Angew Chem Int Ed Engl
; 61(45): e202211000, 2022 Nov 07.
Article
in En
| MEDLINE
| ID: mdl-36031588
ABSTRACT
Whilst 2- or 5-OMe groups on the bridging phenylene ring in [{Cp*(dppe)RuC≡C}2 (µ-1,3-C6 H4 )]+ have little influence on the electronic structure of this weakly coupled mixed-valence complex, a 4-OMe substituent enhances ground state electron delocalization, and increases the intensity of the IVCT transition. Vibrational frequency and TDDFT calculations (LH20t-D3(BJ), def2-SVP, COSMO (CH2 Cl2 )) on ([{Cp*(dppe)RuC≡C}2 (µ-1,3-C6 H3 -n-OMe)]+ (n=2, 4, 5) models are in excellent agreement with the experimental results. The stronger ground state coupling is attributed to the change in composition of the ß-HOSO brought about by the 4-OMe group, which is ortho or para to each of the metal fragments. The intensity of the IVCT transition increases with the greater overlap of the ß-HOSO and ß-LUSO, whilst the relative phases of the ß-HOSO and ß-LUSO in the 4-OMe substituted complex are consistent with predictions of constructive quantum interference from molecular circuit rules.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Angew Chem Int Ed Engl
Year:
2022
Document type:
Article
Affiliation country:
Australia