In:
Zeitschrift für Naturforschung C, Walter de Gruyter GmbH, Vol. 31, No. 5-6 ( 1976-6-1), p. 263-266
Abstract:
The preparation of a new photochemically-activatable polymer was accomplished by condensation of aminohexyl-6-yl-agarose with the N-hydroxysuccinimide ester of 5-azido-2-nitro-benzoic acid. The latter compound was obtained by diazotization of 5-amino-2-nitro-benzoic acid, exchange of the diazonium group through azide and condensation with N-hydroxysuccinimide. As shown for the photolysis on the monomer level, irradiation of the polymer led to the intermediate formation of a highly reactive nitrene, which is able to immobilize ligands e. g. ʟ-phenylalanine to the polymer.
Type of Medium:
Online Resource
ISSN:
1865-7125
,
0939-5075
DOI:
10.1515/znc-1976-5-608
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
1976
detail.hit.zdb_id:
2078107-6
SSG:
12
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