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Conference Paper: Hybrid 1,2,3-Triazole Supported CuII Complexes: Tuning Assembly and Weak Interaction-Driven Crystal Growth

TitleHybrid 1,2,3-Triazole Supported CuII Complexes: Tuning Assembly and Weak Interaction-Driven Crystal Growth
Authors
Issue Date2016
PublisherCSIRO Publishing. The Journal's web site is located at http://www.publish.csiro.au/nid/51.htm
Citation
The 5th Molecular Materials Meeting (M3): The Next 50 Years in Materials Research, Singapore, 3-5 August 2015. In Australian Journal of Chemistry, 2016, v. 69, n. 4, p. 372-378 How to Cite?
Abstract© 2016 CSIRO.Two new dinuclear CuII complexes [Cu2Cl4(L1)2] (1) and [Cu2Cl4(L2)2] (2) (L1=2-((4-(2-(cyclopentylthio)ethyl)-1H-1,2,3-triazol-1-yl)methyl)pyridine; L2=2-((4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl)benzonitrile) were synthesised and characterised by single-crystal X-ray diffraction (XRD), powder XRD, thermogravimetric analysis, elemental analysis and IR measurements. The picolyl-triazole ligand L1 coordinates in a chelate-bridging mode forming a dinuclear structure 1. The more rigid pyridyl-triazole ligand L2 chelates only, generating a chloride-bridged dinuclear complex 2. Both crystals of complexes 1 and 2 show dominant plate shapes that correlate with weak 2D H-bonding interactions in the lattice. A mononuclear structure (3, [CuCl2(L3)2]6H2O, L3 = 3-((4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl)benzonitrile) yields block shape crystals that correlate with 3D H-bonding interactions. This study demonstrates tunable assembly at the molecular level and the relationship of crystal shape with weak lattice interactions.
Persistent Identifierhttp://hdl.handle.net/10722/237527
ISSN
2021 Impact Factor: 1.224
2020 SCImago Journal Rankings: 0.319
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBai, Shi Qiang-
dc.contributor.authorJiang, Lu-
dc.contributor.authorYoung, David James-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2017-01-16T06:09:28Z-
dc.date.available2017-01-16T06:09:28Z-
dc.date.issued2016-
dc.identifier.citationThe 5th Molecular Materials Meeting (M3): The Next 50 Years in Materials Research, Singapore, 3-5 August 2015. In Australian Journal of Chemistry, 2016, v. 69, n. 4, p. 372-378-
dc.identifier.issn0004-9425-
dc.identifier.urihttp://hdl.handle.net/10722/237527-
dc.description.abstract© 2016 CSIRO.Two new dinuclear CuII complexes [Cu2Cl4(L1)2] (1) and [Cu2Cl4(L2)2] (2) (L1=2-((4-(2-(cyclopentylthio)ethyl)-1H-1,2,3-triazol-1-yl)methyl)pyridine; L2=2-((4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl)benzonitrile) were synthesised and characterised by single-crystal X-ray diffraction (XRD), powder XRD, thermogravimetric analysis, elemental analysis and IR measurements. The picolyl-triazole ligand L1 coordinates in a chelate-bridging mode forming a dinuclear structure 1. The more rigid pyridyl-triazole ligand L2 chelates only, generating a chloride-bridged dinuclear complex 2. Both crystals of complexes 1 and 2 show dominant plate shapes that correlate with weak 2D H-bonding interactions in the lattice. A mononuclear structure (3, [CuCl2(L3)2]6H2O, L3 = 3-((4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl)benzonitrile) yields block shape crystals that correlate with 3D H-bonding interactions. This study demonstrates tunable assembly at the molecular level and the relationship of crystal shape with weak lattice interactions.-
dc.languageeng-
dc.publisherCSIRO Publishing. The Journal's web site is located at http://www.publish.csiro.au/nid/51.htm-
dc.relation.ispartofAustralian Journal of Chemistry-
dc.titleHybrid 1,2,3-Triazole Supported CuII Complexes: Tuning Assembly and Weak Interaction-Driven Crystal Growth-
dc.typeConference_Paper-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1071/CH15650-
dc.identifier.scopuseid_2-s2.0-84964388608-
dc.identifier.hkuros285677-
dc.identifier.volume69-
dc.identifier.issue4-
dc.identifier.spage372-
dc.identifier.epage378-
dc.identifier.eissn1445-0038-
dc.identifier.isiWOS:000374182400003-
dc.publisher.placeAustralia-
dc.identifier.issnl0004-9425-

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