Three‐Coordinated Heteroleptic Cu(I) Complexes with Bulky Phosphine Ligands: Influence of Substituents on Photophysical Properties

The design and synthesis of cost‐effective and environmentally friendly luminescent materials have great implications and challenges. In this study, bulky phosphine ligands (Sphos and Xphos) are utilized to synthesize a series of three‐coordinated Cu(I) complexes with different N^N ligands derived from 1,10‐phenanthroline. By employing rigid N^N donor ligands featuring different electron‐donating or withdrawing substituents, the emission from 585 to 698 nm with a microseconds lifetime in the solid state can be systematically modulated. While complexes 1 – 3 with 1,10‐phenanthroline and neocuproine exhibit emission around 590 nm, dicnq (featuring electron‐withdrawing groups) coordinated complexes 4 and 5 exhibit significantly redshifted emissions to ≈700 nm. The experimental and theoretical studies suggest the occurrence of thermally activated delayed fluorescence with microseconds lifetime and a small ΔE ST . This investigation highlights the pivotal role of ligand design in regulating the photophysical characteristics of Cu(I) complexes.

Authors

Institutions

Publication Details

Journal
European Journal of Inorganic Chemistry
Published
2025-10-09
DOI
https://doi.org/10.1002/ejic.202500319
Primary Topic
Metal complexes synthesis and properties
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Three‐Coordinated Heteroleptic Cu(I) Complexes with Bulky Phosphine Ligands: Influence of Substituents on Photophysical Properties

Soumen Ghosh, Lydie Viau, Abhinav Raghuvanshi, Laxman Sarjerao Kharabe et al.
European Journal of Inorganic Chemistry
Metal complexes synthesis and properties
article

Three‐Coordinated Heteroleptic Cu(I) Complexes with Bulky Phosphine Ligands: Influence of Substituents on Photophysical Properties

Soumen Ghosh, Lydie Viau, Abhinav Raghuvanshi, Laxman Sarjerao Kharabe, Jyoti Pannu
article en

Abstract

The design and synthesis of cost‐effective and environmentally friendly luminescent materials have great implications and challenges. In this study, bulky phosphine ligands (Sphos and Xphos) are utilized to synthesize a series of three‐coordinated Cu(I) complexes with different N^N ligands derived from 1,10‐phenanthroline. By employing rigid N^N donor ligands featuring different electron‐donating or withdrawing substituents, the emission from 585 to 698 nm with a microseconds lifetime in the solid state can be systematically modulated. While complexes 1 – 3 with 1,10‐phenanthroline and neocuproine exhibit emission around 590 nm, dicnq (featuring electron‐withdrawing groups) coordinated complexes 4 and 5 exhibit significantly redshifted emissions to ≈700 nm. The experimental and theoretical studies suggest the occurrence of thermally activated delayed fluorescence with microseconds lifetime and a small ΔE ST . This investigation highlights the pivotal role of ligand design in regulating the photophysical characteristics of Cu(I) complexes.

European Journal of Inorganic ChemistryVol. 28(30)
Indian Institute of Technology Madras (IN), Institut UTINAM (FR), Université Marie et Louis Pasteur (FR), Indian Institute of Technology Indore (IN)
Openalex Percentile: Top 61%
Metal complexes synthesis and properties
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Three‐Coordinated Heteroleptic Cu(I) Complexes with Bulky Phosphine Ligands: Influence of Substituents on Photophysical Properties — Soumen Ghosh, Lydie Viau, et al. · European Journal of Inorganic Chemistry (2025) | TGRS Research Map | TGRS