Single-Crystal to Single-Crystal Transformation of a 0D Cu(II) Metallocycle into a 1D Coordination Polymer Triggered by Spontaneous Desolvation in Mother Liquor

4Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A novel Cu(II) imidazolyl-based metallocycle, [Cu2L12(NO3)4]·2MeCN, undergoes a single-crystal to single-crystal transformation to form a 1D coordination polymer, [CuL1(NO3)2]n. This transformation is triggered by the loss of solvent in the presence of the same solvent, which is counterintuitive. Expulsion of interstitial solvent molecules occurs with concomitant rearrangement of the ligands, which concertedly recoordinate to nearby metal centers to achieve a lower energy state. This is the first imidazolyl-based metallacycle reported to undergo such a phase transformation.

Cite

CITATION STYLE

APA

Wei, X., de Beer, S., & Barbour, L. J. (2023). Single-Crystal to Single-Crystal Transformation of a 0D Cu(II) Metallocycle into a 1D Coordination Polymer Triggered by Spontaneous Desolvation in Mother Liquor. Crystal Growth and Design, 23(9), 6258–6262. https://doi.org/10.1021/acs.cgd.3c00644

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free