Single cyanide-bridged Mo(W)/S/Cu cluster-based coordination polymers: Reactant- and stoichiometry-dependent syntheses, effective photocatalytic properties
Creators
- 1. China-Australia Joint Research Center for Functional Molecular Materials, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122 (China)
- 2. China-Australia Joint Research Center for Functional Molecular Materials, Scientific Research Academy, Jiangsu University, Zhenjiang 212013 (China)
- 3. Research School of Chemistry, Australian National University, Canberra ACT 0200 (Australia)
Description
The systematic study on the reaction variables affecting single cyanide-bridged Mo(W)/S/Cu cluster-based coordination polymers (CPs) is firstly demonstrated. Five anionic single cyanide-bridged Mo(W)/S/Cu cluster-based CPs {[Pr4N][WS4Cu3(CN)2]}n (1), {[Pr4N][WS4Cu4(CN)3]}n (2), {[Pr4N][WOS3Cu3(CN)2]}n (3), {[Bu4N][WOS3Cu3(CN)2]}n (4) and {[Bu4N][MoOS3Cu3(CN)2]}n (5) were prepared by varying the molar ratios of the starting materials, and the specific cations, cluster building blocks and central metal atoms in the cluster building blocks. 1 possesses an anionic 3D diamondoid framework constructed from 4-connected T-shaped clusters [WS4Cu3]+ and single CN− bridges. 2 is fabricated from 6-connected planar 'open' clusters [WS4Cu4]2+ and single CN− bridges, forming an anionic 3D architecture with an "ACS" topology. 3 and 4 exhibit novel anionic 2-D double-layer networks, both constructed from nest-shaped clusters [WOS3Cu3]+ linked by single CN− bridges, but containing the different cations [Pr4N]+ and [Bu4N]+, respectively. 5 is constructed from nest-shaped clusters [MoOS3Cu3]+ and single CN− bridges, with an anionic 3D diamondoid framework. The anionic frameworks of 1-5, all sustained by single CN− bridges, are non-interpenetrating and exhibit huge potential void volumes. Employing differing molar ratios of the reactants and varying the cluster building blocks resulted in differing single cyanide-bridged Mo(W)/S/Cu cluster-based CPs, while replacing the cation ([Pr4N]+ vs. [Bu4N]+) was found to have negligible impact on the nature of the architecture. Unexpectedly, replacement of the central metal atom (W vs. Mo) in the cluster building blocks had a pronounced effect on the framework. Furthermore, the photocatalytic activities of heterothiometallic cluster-based CPs were firstly explored by monitoring the photodegradation of methylene blue (MB) under visible light irradiation, which reveals that 2 exhibits effective photocatalytic properties. - Highlights: • Reaction variables affecting Mo(W)/S/Cu cluster-based CPs is firstly explored. • Replacing central metal atom had a pronounced effect on W/S/Cu cluster-based CPs. • Photocatalytic activities of Mo(W)/S/Cu cluster-based CPs are firstly investigated.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2015.08.025Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2015.08.025;
- PII
- S0022-4596(15)30127-4;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry
- Journal Volume
- 231
- Journal Page Range
- p. 230-238
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48018197
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CATIONS; COPPER COMPOUNDS; CYANIDES; IRRADIATION; LAYERS; METALS; METHYLENE BLUE; MOLYBDENUM COMPLEXES; MONITORING; PHOTOCATALYSIS; POLYMERS; SULFUR COMPOUNDS; SYNTHESIS
- Descriptors DEC
- AMINES; ANTI-INFECTIVE AGENTS; ANTIMICROBIAL AGENTS; AZINES; CATALYSIS; CHARGED PARTICLES; CHLORIDES; CHLORINE COMPOUNDS; COMPLEXES; DRUGS; ELEMENTS; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC COMPOUNDS; IONS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; PHENOTHIAZINES; TRANSITION ELEMENT COMPLEXES; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.