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The Structures of Tetramethylrhodamine Isothiocyanate Isomers: An N. M. R. Study

 

作者: D. Kramer,   H. Klapper,   F. Miller,  

 

期刊: Spectroscopy Letters  (Taylor Available online 1968)
卷期: Volume 1, issue 1  

页码: 23-26

 

ISSN:0038-7010

 

年代: 1968

 

DOI:10.1080/00387016808049939

 

出版商: Taylor & Francis Group

 

关键词: tetramethylrhodamine;isothiocyanate;n. m. r. study

 

数据来源: Taylor

 

摘要:

The use of tetramethylrhodamine isothiocyanate isomers R and G in microbiological and immunochemical procedures has prompted interest in their chemical and physical properties. Tetramethylrhodamine isothiocyanate (TMR) isomer R has been found to be more efficacious than isomer G in immunochemical work (1). Hence, the establishment of the structures of the respective isomers of tetramethylrhodamine isothiocyanates (Figure II) would be of value for better understanding the fluorescent staining and immunochemical activities of these reagents.

 

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