Document Detail


Mass spectral fragmentation patterns of some new 3,7-dichloro-benzo[1,2-b:4,5-b']dithiophene-2,6-dicarboxylic acid dianilides and 3,5-dichloro-dithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxylic acid dianilides. II.
MedLine Citation:
PMID:  7766914     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The electron impact mass spectra of some benzo[1,2-b:4,5-b']dithiophene-2,6-dicarboxylic acid dianilides and dithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxylic acid dianilides are discussed. Dominant peaks in these dianilides are formed by the cleavage of a C-N bond on one side of an anilino group. These ions fragment further by the cleavage of a C-C bond on the other side of an anilino group and a CONRPhR' group may be lost directly. After loss of CO, the characteristic benzodithiophene radical cation, C10H2S2Cl2[symbol: see text], at m/z 256 and the dithienothiophene radical cation, C8S3Cl2[symbol: see text], at m/z 262 are formed from their respective precursor compounds.
Authors:
G Karminski-Zamola; M Malesević; N Blazević; M Bajić; D W Boykin
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Rapid communications in mass spectrometry : RCM     Volume:  9     ISSN:  0951-4198     ISO Abbreviation:  Rapid Commun. Mass Spectrom.     Publication Date:  1995  
Date Detail:
Created Date:  1995-07-05     Completed Date:  1995-07-05     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8802365     Medline TA:  Rapid Commun Mass Spectrom     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  400-4     Citation Subset:  IM    
Affiliation:
Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Croatia.
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MeSH Terms
Descriptor/Qualifier:
Anilides / analysis*
Dicarboxylic Acids / analysis*
Gas Chromatography-Mass Spectrometry*
Thiophenes / analysis*
Grant Support
ID/Acronym/Agency:
R03 TW00249/TW/FIC NIH HHS
Chemical
Reg. No./Substance:
0/Anilides; 0/Dicarboxylic Acids; 0/Thiophenes

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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