Template syntheses of diverse haloargentates with reversible photochromism behaviors and efficient photocatalytic properties

By virtue of the template synthesis strategy, a series of haloargentates [Me-hmta][AgI 2 ]·H 2 O ( 1 ), [Me-hmta][Ag 2 I 3 ] ( 2 ) and [Me-hmta][Ag 2 Br 3 ] ( 3 ) (hmta = hexamethylenetetramine), have been successfully prepared. Compounds 1-3 feature diverse infinite chains with in situ methylated M...

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Bibliographic Details
Published inCrystEngComm Vol. 23; no. 7; pp. 1588 - 1595
Main Authors Xue, Zhen-Zhen, Wang, A-Ni, Wei, Qi, Wei, Li, Han, Song-De, Pan, Jie
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 22.02.2021
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Summary:By virtue of the template synthesis strategy, a series of haloargentates [Me-hmta][AgI 2 ]·H 2 O ( 1 ), [Me-hmta][Ag 2 I 3 ] ( 2 ) and [Me-hmta][Ag 2 Br 3 ] ( 3 ) (hmta = hexamethylenetetramine), have been successfully prepared. Compounds 1-3 feature diverse infinite chains with in situ methylated Me-hmta cations serving as the templates and structure-directing agents. The syntheses, crystal structures and characterizations have been investigated for the compounds. Interestingly, compounds 1 and 2 exhibit the reversible photo-induced chromic behaviors. The solid samples can be colored with light illumination and further decolored in the presence of heat. Moreover, photocatalysis tests have been performed on 2 and 3 , which display that the compounds can be considered as promising photocatalysts with high efficiency toward the degradation of organic dye pollutants. A series of haloargentates have been prepared exhibiting a reversible photochromic phenomenon and efficient photocatalytic properties.
Bibliography:PXRD, IR and ESR curves for compounds
for compounds
and UV-vis spectra for methyl blue in the presence of compounds
Electronic supplementary information (ESI) available: Selected bond distances and angles for compounds
1-3
2-3
10.1039/d0ce01642j
2033656-2033658
CCDC numbers are
respectively. For ESI and crystallographic data in CIF or other electronic format see DOI
ISSN:1466-8033
1466-8033
DOI:10.1039/d0ce01642j