Phosphine-substituted diiron complexes Fe<sub>2</sub>(<i>μ</i>-Rodt)(CO)<sub>6−<i>n</i></sub>(PPh<sub>3</sub>)<sub><i>n</i></sub>(R = Ph, Me, H and<i>n</i>= 1, 2) featuring desymmetrized oxadithiolate bridges: structures, protonation, and electrocatalysis - Concepedia

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Phosphine-substituted diiron complexes Fe<sub>2</sub>(<i>μ</i>-Rodt)(CO)<sub>6−<i>n</i></sub>(PPh<sub>3</sub>)<sub><i>n</i></sub>(R = Ph, Me, H and<i>n</i>= 1, 2) featuring desymmetrized oxadithiolate bridges: structures, protonation, and electrocatalysis

11

Citations

50

References

2021

Year

Xiaoli Gu, Jian‐Rong Li, Bo Jin, Yang Guo, Xing‐Bin Jing, Pei‐Hua Zhao

New Journal of Chemistry

Abstract

The influence of desymmetrized dithiolates (Rodt) and phosphine coordination modes (PPh 3 ) on the structural, protophilic, and electrocatalytic features of diiron complexes 4–6 and 7–9 is described.

References

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