Structural,PhotoluminescentandTheoreticalEvidenceforLigand-unsupportedArgentophilicInteractionsinaSupramolecularAggregateof[Ag2(Hida)(NH3)2]

被引:2
作者
郑绍良
杨锦华
陈小明
机构
[1] MOELaboratoryofBioinorganicandSyntheticChemistry,SchoolofChemistryandChemicalEngineering,SunYat-SenUniversity
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中图分类号
O627.12 [铜族金属有机化合物];
学科分类号
070303 ; 081704 ;
摘要
A new neutral [Ag2(Hida)(NH3)2] molecule (1, H3ida = 1H-imidazole-4,5-dicarboxy- lic acid) has been synthesized and structurally characterized by single-crystal diffraction. Compound 1 crystallizes in monoclinic, space group C2/c with a = 18.3928(8), b = 8.3299(5), c = 13.682(7) , β = 113.179(2)o, V = 1926.9(10)3, Z = 8 and Dc = 2.784 g·cm-3. In the solid state, this disilver(I) compound can aggregate to furnish the energetically stable ligand-unsupported AgI–AgI interaction concomitant with significant photoluminescence changes in different aggregate states, and such argentophilicity interaction is also supported by molecular orbital calculations.
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页码:1503 / 1508
页数:6
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