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dc.contributor.authorKullapa Chanawannoen_US
dc.contributor.authorCole Holstromen_US
dc.contributor.authorLaura A. Crandallen_US
dc.contributor.authorHenry Dodgeen_US
dc.contributor.authorVictor N. Nemykinen_US
dc.contributor.authorRichard S. Herricken_US
dc.contributor.authorChristopher J. Ziegleren_US
dc.date.accessioned2018-09-05T02:56:56Z-
dc.date.available2018-09-05T02:56:56Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn14779234en_US
dc.identifier.issn14779226en_US
dc.identifier.other2-s2.0-84987778387en_US
dc.identifier.other10.1039/c6dt02669aen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84987778387&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55482-
dc.description.abstract© 2016 The Royal Society of Chemistry. A series of 1,1′-bis(sulfonyl)ferrocene compounds were produced via the 1,1′-bis(sulfonate)ferrocene ammonium salt. This compound can be readily converted to 1,1′ bis(sulfonylchloride)ferrocene. By varying stoichiometry and reaction times, both mono- and bis-sulfonamide derivatives can be synthesized. All new compounds presented in this report have been structurally characterized. The structures of the bis-sulfonamide systems are similar to the well-studied bis(amide) ferrocene compounds. Intermolecular hydrogen bonding is observed, typically between NH and SO groups of neighboring sulfonamides. However in the bis(GABA) derivative, intermolecular NH to CO hydrogen bonding interactions are present.en_US
dc.subjectChemistryen_US
dc.titleThe synthesis and structures of 1,1′-bis(sulfonyl)ferrocene derivativesen_US
dc.typeJournalen_US
article.title.sourcetitleDalton Transactionsen_US
article.volume45en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Minnesota Duluthen_US
article.stream.affiliationsUniversity of Akronen_US
article.stream.affiliationsCollege of the Holy Crossen_US
Appears in Collections:CMUL: Journal Articles

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