Affiliation:
1. Department of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, China
2. State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China
Abstract
So far, the development of new iodoargentate-based hybrids, especially those compounds with metal complex cations, and the understanding of their structure–activity relationships have been of vital importance but full of challenges. Herein, using the in-situ-generated metal complex cations as structural directing agents, three new iodoargentate-based hybrids, namely, [Co(phen)3]Ag2PbI6 (phen = 1,10-phenanthroline; 1), [Ni(5,5-dmpy)3]Ag7I9·CH3CN (5,5-dmpy = 5,5-dimethyl-2,2-bipyridine; 2) and [Co(5,5-dmpy)3]Ag5I8 (3), have been solvothermally prepared and then structurally characterized. Compound 1 represents one new heterometallic Ag–Pb–I compound characteristic of the chain-like [Ag2PbI6]n2n− anions. Compound 2 features the straight one-dimensional (1D) [Ag7I9]n2n− anionic moieties, while compound 3 contains infrequent two types of curved [Ag5I8]n3n− anions. Optical properties reveal that the title compounds exhibit interesting semiconductor behaviors with the band gaps of 1.59–2.78 eV, which endow them with good photoelectric switching performances under the alternate light irradiations. We also present their Hirshfeld surface analyses, and the theoretical studies (band structures, density of states (DOS) and partial density of states (PDOS)).
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Cited by
4 articles.
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