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Single-Crystal to Single-Crystal Transformation of a 0D Cu(II) Metallocycle into a 1D Coordination Polymer Triggered by Spontaneous Desolvation in Mother Liquor
被引:2
|作者:
Wei, Xueting
[1
]
de Beer, Shane
[1
]
Barbour, Leonard J. J.
[1
]
机构:
[1] Stellenbosch Univ, Dept Chem & Polymer Sci, ZA-7602 Matieland, South Africa
基金:
新加坡国家研究基金会;
关键词:
ORGANIC FRAMEWORK MATERIALS;
GUEST REMOVAL;
METAL;
INTERPENETRATION;
EXCHANGE;
COMPLEX;
D O I:
10.1021/acs.cgd.3c00644
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A novel 0D Cu(II) dinuclear imidazolyl-based metallocycledesolvates in the presence of mother liquor and transforms into a1D coordination polymer in a single-crystal to single-crystal fashion.The mechanism of this transformation has been elucidated, and structuralfeatures responsible for this transformation have been identified. A novel Cu(II) imidazolyl-based metallocycle, [Cu(2)L1(2)(NO3)(4)]& BULL;2MeCN, undergoesa single-crystalto single-crystal transformation to form a 1D coordination polymer,[CuL1(NO3)(2)]( n ). Thistransformation is triggered by the loss of solvent in the presenceof the same solvent, which is counterintuitive. Expulsion of interstitialsolvent molecules occurs with concomitant rearrangement of the ligands,which concertedly recoordinate to nearby metal centers to achievea lower energy state. This is the first imidazolyl-based metallacyclereported to undergo such a phase transformation.
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页码:6258 / 6262
页数:5
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