Triptycene-based diiron(<scp>ii</scp>) mesocates: spin-crossover in solution-Reference-Cited by-同舟云学术

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Triptycene-based diiron(ii) mesocates: spin-crossover in solution

Published:2024 Issue:42 Volume:60 Page:5522-5525
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Mobili Riccardo¹²^ORCID,Preda Giovanni¹^ORCID,Dondi Daniele¹^ORCID,Monzani Enrico¹^ORCID,Vadivel Dhanalakshmi¹^ORCID,Massera Chiara³^ORCID,Pasini Dario¹^ORCID,Amendola Valeria¹^ORCID

Affiliation:

1. Department of Chemistry, University of Pavia, viale Torquato Taramelli 12, 27100 Pavia, Italy

2. Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, 4 Place Jussieu, Paris, France

3. Department of Chemistry, Life Science and Environmental Sustainability University of Parma, Parco Area delle Scienze 17/A, 43124, Parma, Italy

Abstract

A triptycene-based diiron(ii) mesocate, synthesized using a rigid ligand containing two pyridylbenzimidazole chelating units, exhibited thermal-induced spin-crossover behaviour in solution.

Funder

Ministero dell'Università e della Ricerca

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC00812J

Reference47 articles.

1. Iptycenes in supramolecular and materials chemistry

2. Iptycenes in the Design of High Performance Polymers

3. Triptycene-Derived Macrocyclic Arenes: From Calixarenes to Helicarenes

4. Triptycene Derivatives: From Their Synthesis to Their Unique Properties

5. Triptycene End‐Capping as Strategy in Materials Chemistry to Control Crystal Packing and Increase Solubility

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