Origin of a counterintuitive yellow light-emitting electrochemical cell based on a blue-emitting heteroleptic copper(i) complex-Reference-Cited by-同舟云学术

Origin of a counterintuitive yellow light-emitting electrochemical cell based on a blue-emitting heteroleptic copper(i) complex

Published:2016 Issue:21 Volume:45 Page:8984-8993
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Weber Michael D.¹²³⁴,Garino Claudio⁵⁶⁷⁸,Volpi Giorgio⁵⁶⁷⁸,Casamassa Enrico⁵⁶⁷⁸,Milanesio Marco⁹¹⁰¹¹⁸,Barolo Claudia⁵⁶⁷⁸,Costa Rubén D.¹²³⁴

Affiliation:

1. Department of Physical Chemistry 1

2. University of Erlangen-Nürnberg

3. 91058 Erlangen

4. Germany

5. Department of Chemistry and NIS Interdepartmental Centre

6. University of Torino

7. 10125 Torino

8. Italy

9. Dipartimento di Scienze e Innovazione and CrisDi Interdepartmental Center for Crystallography

10. Università del Piemonte Orientale Tecnologica

11. 15121 Alessandria

Abstract

A new copper(i) complex, which lacks of charge transfer character in the excited state, features a blue fluorescence and yellow phosphorescence photo- and electro-responses, respectively.

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/DT/C6DT00970K

Reference55 articles.

1. From iridium and platinum to copper and carbon: new avenues for more sustainability in organic light-emitting diodes

2. Diversity of Copper(I) Complexes Showing Thermally Activated Delayed Fluorescence: Basic Photophysical Analysis

3. Thermally Activated Delayed Fluorescence Materials Towards the Breakthrough of Organoelectronics

4. Highly Efficient Green Organic Light-Emitting Diodes Containing Luminescent Three-Coordinate Copper(I) Complexes

5. Highly efficient cuprous complexes with thermally activated delayed fluorescence and simplified solution process OLEDs using the ligand as host

Cited by 99 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Nitration of Derivatives of Imidazo[1,5‐a]pyridine via C−H Functionalization with Fe(NO₃)₃ ⋅ 9H₂O as a Promoter and a Nitro Source;ChemistrySelect;2024-06-18

2. Imidazo[1,2-a]pyridine and Imidazo[1,5-a]pyridine: Electron Donor Groups in the Design of D–π–A Dyes;The Journal of Organic Chemistry;2024-06-10

3. Imidazopyridine Family: Versatile and Promising Heterocyclic Skeletons for Different Applications;Molecules;2024-06-05

4. Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN₃ Using O₂ as the Oxygen Source;The Journal of Organic Chemistry;2024-04-01

5. Highly Versatile Preparation of Imidazo[1,5‐a]quinolines and Characterization of Their Photoluminescent Properties;European Journal of Organic Chemistry;2023-12-19