Synthesis and degradation of photolabile dendrimers based on o-nitrobenzyl ether photolabile cores

Robert M. Kevwitch, Dominic V Mcgrath

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Two dendrimer cores, 1a and 2a, that contain o-nitrobenzyl photolabile moieties, lack hydrolytically sensitive ester linkages and possess three and six sites for dendron attachment, respectively, have been alkylated to provide methylated core analogs 1b and 2b as well as second-generation benzylaryl ether dendrimer 1c and third-generation dendrimer 2c. These dendrimers undergo clean photocleavage as indicated by the evolution of isosbestic points in the UV spectra during photolysis. In addition, the nature of the photodegradation products was confirmed by observing the photolyses by both 1H NMR and GPC.

Original languageEnglish (US)
Pages (from-to)1332-1336
Number of pages5
JournalNew Journal of Chemistry
Volume31
Issue number7
DOIs
StatePublished - 2007

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Dendrimers
Ether
Ethers
Degradation
Photolysis
Photodegradation
Esters
Nuclear magnetic resonance

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Synthesis and degradation of photolabile dendrimers based on o-nitrobenzyl ether photolabile cores. / Kevwitch, Robert M.; Mcgrath, Dominic V.

In: New Journal of Chemistry, Vol. 31, No. 7, 2007, p. 1332-1336.

Research output: Contribution to journalArticle

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