Impact of a conformationally restricted receptor on the BF2 chelated azadipyrromethene fluorosensing platform
Authors:
- 27 February 2006
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 14,p. 1503-1505
Abstract
Conformational control of the receptor–fluorophore orientation of BF2 chelated azadipyrromethene sensors reveals two photophysically different modes of analyte triggered fluorescence switching both of which exhibit large off–on fluorescence intensity responses to the light input–output of the sensors in the visible red spectral region.Keywords
This publication has 28 references indexed in Scilit:
- Looking and listening to light: the evolution of whole-body photonic imagingNature Biotechnology, 2005
- Heptamethine Cyanine Dyes with a Large Stokes Shift and Strong Fluorescence: A Paradigm for Excited-State Intramolecular Charge TransferJournal of the American Chemical Society, 2005
- Proton controlled intramolecular photoinduced electron transfer (PET) in podand linked squaraine–aniline dyadsChemical Communications, 2004
- Boron–Diindomethene (BDI) Dyes and Their Tetrahydrobicyclo Precursors—en Route to a New Class of Highly Emissive Fluorophores for the Red Spectral RangeChemistry – A European Journal, 2004
- Molecular imaging in drug discovery and developmentNature Reviews Drug Discovery, 2003
- An Azulene Dimer as a Near-Infrared QuencherAngewandte Chemie International Edition, 2002
- Scaling down imaging: molecular mapping of cancer in miceNature Reviews Cancer, 2002
- Turning the spotlight on cellular imagingNature Biotechnology, 2001
- Infrared fluorescence sensing of submicromolar calcium: pushing the limits of photoinduced electron transferTetrahedron Letters, 2000
- One-Pot Synthesis of Squaraine FluoroionophoresThe Journal of Organic Chemistry, 1998