Literature DB >> 15346183

Photoremovable protecting groups based on electron transfer chemistry.

Daniel E Falvey1, Chitra Sundararajan.   

Abstract

Photoremovable protecting groups (also known as photolabile protecting groups, phototriggers, or caged molecules) are functional groups that are attached to a molecule in such a way as to render the latter inactive. Exposure to light releases the protecting group, restoring functionality to the molecule. The use of photoremovable protecting groups (PRPGs) allows for precise spatial and temporal control of chemical reactions. Such groups have found use in many diverse applications, ranging from time resolved studies of physiological processes, to fabrication of spatially resolved combinatorial libraries of DNA. Recent research efforts have focused on designing protecting groups that are removed through photoinduced electron transfer (PET), rather than by direct photolysis. The PET strategy allows the light absorption step to be decoupled from the bond breaking step, thus permitting more control over the wavelengths of light used in the release process. The application of these types of protecting groups to the photochemical release of amines, alcohols, ketones, and carboxylic acids is described.

Entities:  

Year:  2004        PMID: 15346183     DOI: 10.1039/b406866a

Source DB:  PubMed          Journal:  Photochem Photobiol Sci        ISSN: 1474-905X            Impact factor:   3.982


  5 in total

Review 1.  Photoremovable protecting groups in chemistry and biology: reaction mechanisms and efficacy.

Authors:  Petr Klán; Tomáš Šolomek; Christian G Bochet; Aurélien Blanc; Richard Givens; Marina Rubina; Vladimir Popik; Alexey Kostikov; Jakob Wirz
Journal:  Chem Rev       Date:  2012-12-21       Impact factor: 60.622

2.  Visible-to-NIR-Light Activated Release: From Small Molecules to Nanomaterials.

Authors:  Roy Weinstain; Tomáš Slanina; Dnyaneshwar Kand; Petr Klán
Journal:  Chem Rev       Date:  2020-10-30       Impact factor: 60.622

3.  Electronic structures and spin topologies of gamma-picoliniumyl radicals. A study of the homolysis of N-methyl-gamma-picolinium and of benzo-, dibenzo-, and naphthoannulated analogs.

Authors:  Rainer Glaser; Yongqiang Sui; Ujjal Sarkar; Kent S Gates
Journal:  J Phys Chem A       Date:  2008-05-29       Impact factor: 2.781

4.  Two-photon sensitive protecting groups operating via intramolecular electron transfer: uncaging of GABA and tryptophan.

Authors:  Karolina A Korzycka; Philip M Bennett; Eduardo Jose Cueto-Diaz; Geoffrey Wicks; Mikhail Drobizhev; Mireille Blanchard-Desce; Aleksander Rebane; Harry L Anderson
Journal:  Chem Sci       Date:  2015-02-03       Impact factor: 9.825

5.  Near-infrared uncaging or photosensitizing dictated by oxygen tension.

Authors:  Erin D Anderson; Alexander P Gorka; Martin J Schnermann
Journal:  Nat Commun       Date:  2016-11-17       Impact factor: 14.919

  5 in total

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