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Article: Quinoneimido complexes of a metalloporphyrin: Isolation, X-ray crystal structures, and DFT calculations

TitleQuinoneimido complexes of a metalloporphyrin: Isolation, X-ray crystal structures, and DFT calculations
Authors
Tsui, WMHuang, JSTong, GSMKui, SCFChe, CMZhu, N
KeywordsDensity functional calculations
N ligands
Porphyrins
Quinoneimido complexes
Ruthenium
Issue Date2010
PublisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/publish/en/journals/alphabeticIndex/2451
Citation
Chemistry - An Asian Journal, 2010, v. 5 n. 4, p. 759-763 How to Cite?
DOI: http://dx.doi.org/10.1002/asia.200900666
AbstractTerminal quinoneimido complexes [RuIV (por) (NQu)(X)] (X=OEt: 1, OH: 2) were formed from the reaction of [Ru VI(por)O2] with 2,6-dimethylaniline. The X-ray crystal structures of 1 feature Ru-N(quinoneimido) bond lengths of 1.787(7)-1.80(2). Reaction of 2 with N-phenyl-benzene-1,4-diamine afforded bis(quinoneimido) complex [Ru(por) (NQu) (NQu')]. DFT calculations on 3 and 4 revealed a significant effect of 'Ru doping' on the oligoaniline structure. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Persistent Identifierhttp://hdl.handle.net/10722/134716
ISSN
1861-4728
2023 Impact Factor: 3.5
2023 SCImago Journal Rankings: 0.846
ISI Accession Number ID
WOS:000276641400004
Funding AgencyGrant Number
The University of Hong Kong (University Development Fund)
Hong Kong Research Grants CouncilHKU 1/CRF/08
University Grants Committee of the Hong Kong SAR of ChinaAoE/P-10/01
Funding Information:

This work was supported by The University of Hong Kong (University Development Fund), the Hong Kong Research Grants Council (HKU 1/CRF/08), and the University Grants Committee of the Hong Kong SAR of China (Area of Excellence Scheme, AoE/P-10/01).

References
References in Scopus
Grants
Institute of molecular technology for drug discovery and synthesis

 

DC FieldValueLanguage
dc.contributor.authorTsui, WMen_HK
dc.contributor.authorHuang, JSen_HK
dc.contributor.authorTong, GSMen_HK
dc.contributor.authorKui, SCFen_HK
dc.contributor.authorChe, CMen_HK
dc.contributor.authorZhu, Nen_HK
dc.date.accessioned2011-07-08T07:39:00Z-
dc.date.available2011-07-08T07:39:00Z-
dc.date.issued2010en_HK
dc.identifier.citationChemistry - An Asian Journal, 2010, v. 5 n. 4, p. 759-763en_HK
dc.identifier.issn1861-4728en_HK
dc.identifier.urihttp://hdl.handle.net/10722/134716-
dc.description.abstractTerminal quinoneimido complexes [RuIV (por) (NQu)(X)] (X=OEt: 1, OH: 2) were formed from the reaction of [Ru VI(por)O2] with 2,6-dimethylaniline. The X-ray crystal structures of 1 feature Ru-N(quinoneimido) bond lengths of 1.787(7)-1.80(2). Reaction of 2 with N-phenyl-benzene-1,4-diamine afforded bis(quinoneimido) complex [Ru(por) (NQu) (NQu')]. DFT calculations on 3 and 4 revealed a significant effect of 'Ru doping' on the oligoaniline structure. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.en_HK
dc.languageeng-
dc.publisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/publish/en/journals/alphabeticIndex/2451en_HK
dc.relation.ispartofChemistry - An Asian Journalen_HK
dc.subjectDensity functional calculationsen_HK
dc.subjectN ligandsen_HK
dc.subjectPorphyrinsen_HK
dc.subjectQuinoneimido complexesen_HK
dc.subjectRutheniumen_HK
dc.titleQuinoneimido complexes of a metalloporphyrin: Isolation, X-ray crystal structures, and DFT calculationsen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1861-4728&volume=5&issue=4&spage=759&epage=763&date=2010&atitle=Quinoneimido+complexes+of+a+metalloporphyrin:+isolation,+X-ray+crystal+structures,+and+DFT+calculations-
dc.identifier.emailHuang, JS: jshuang@hku.hken_HK
dc.identifier.emailTong, GSM: tongsm@hku.hken_HK
dc.identifier.emailKui, SCF: stevenku@hku.hken_HK
dc.identifier.emailChe, CM: cmche@hku.hken_HK
dc.identifier.emailZhu, N: nzhu@hkucc.hku.hken_HK
dc.identifier.authorityHuang, JS=rp00709en_HK
dc.identifier.authorityTong, GSM=rp00790en_HK
dc.identifier.authorityKui, SCF=rp00715en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.identifier.authorityZhu, N=rp00845en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/asia.200900666en_HK
dc.identifier.pmid20127788-
dc.identifier.scopuseid_2-s2.0-77950811193en_HK
dc.identifier.hkuros170898-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-77950811193&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume5en_HK
dc.identifier.issue4en_HK
dc.identifier.spage759en_HK
dc.identifier.epage763en_HK
dc.identifier.isiWOS:000276641400004-
dc.publisher.placeGermanyen_HK
dc.relation.projectInstitute of molecular technology for drug discovery and synthesis-
dc.identifier.scopusauthoridTsui, WM=36000681700en_HK
dc.identifier.scopusauthoridHuang, JS=7407192639en_HK
dc.identifier.scopusauthoridTong, GSM=7102328656en_HK
dc.identifier.scopusauthoridKui, SCF=6506763660en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.scopusauthoridZhu, N=7201449530en_HK
dc.identifier.issnl1861-471X-

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