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BODIPY-derived photoremovable protecting groups unmasked with green light.
Goswami, Pratik P; Syed, Aleem; Beck, Christie L; Albright, Toshia R; Mahoney, Kaitlyn M; Unash, Ryan; Smith, Emily A; Winter, Arthur H.
Afiliação
  • Goswami PP; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Syed A; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Beck CL; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Albright TR; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Mahoney KM; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Unash R; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Smith EA; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
  • Winter AH; Department of Chemistry, Iowa State University, 2101d Hach Hall, Ames, Iowa 50011, United States.
J Am Chem Soc ; 137(11): 3783-6, 2015 Mar 25.
Article em En | MEDLINE | ID: mdl-25751156
ABSTRACT
Photoremovable protecting groups derived from meso-substituted BODIPY dyes release acetic acid with green wavelengths >500 nm. Photorelease is demonstrated in cultured S2 cells. The photocaging structures were identified by our previously proposed strategy of computationally searching for carbocations with low-energy diradical states as a possible indicator of a nearby productive conical intersection. The superior optical properties of these photocages make them promising alternatives to the popular o-nitrobenzyl photocage systems.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article