fulltext.study @t Gmail

Photostabilities of novel heptamethine 3H-indolenine cyanine dyes with different N-substituents

Paper ID Volume ID Publish Year Pages File Format Full-Text
29119 44122 2006 7 PDF Available
Title
Photostabilities of novel heptamethine 3H-indolenine cyanine dyes with different N-substituents
Abstract

Novel near-infrared (NIR) 3H-indocyanine dyes with different N-substituents were synthesized and tested to make clear the relationship between photophysical properties and structures and develop potential NIR cyanine dyes with high photostability for fluorescent imaging technology. The electron-withdrawing ability of the substituents on N-position of 3H-indolenine strongly affects the photostabilities of the NIR cyanine dyes and introducing of the electron-donating groups is favorable to obtain NIR cyanine dyes with improved photochemical stability.

Keywords
Near-infrared cyanine dye; Photostability; Fluorescence quantum yield; Photobleaching; Fluorescence labeling
First Page Preview
Photostabilities of novel heptamethine 3H-indolenine cyanine dyes with different N-substituents
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us
Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Photochemistry and Photobiology A: Chemistry - Volume 181, Issue 1, 5 July 2006, Pages 79–85
Authors
, , , , , ,
Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us