Compounds > tris(4-7-diphenyl-1-10-phenanthroline)ruthenium-(ii)

tris(4-7-diphenyl-1-10-phenanthroline)ruthenium-(ii) and carbostyril

tris(4-7-diphenyl-1-10-phenanthroline)ruthenium-(ii) has been researched along with carbostyril* in 1 studies

Other Studies

1 other study(ies) available for tris(4-7-diphenyl-1-10-phenanthroline)ruthenium-(ii) and carbostyril

Article	Year
Photophysical characterization of a FRET system using tailor-made DNA oligonucleotide sequences. Bioconjugate chemistry, 2010, Dec-15, Volume: 21, Issue:12 We have carried out a detailed photophysical study of the FRET D/A pair consisting of a carbostyril donor and a Ru(II)bathophenanthroline complex acceptor in double-stranded synthetic DNA. Altogether 13 different double-stranded 30 base pair DNAs showing small incremental differences in the distances between donor and acceptor were synthesized. Using the fluorescence of the donor as well as of the acceptor, D/A separations were determined and compared to those derived from a well-established model for DNA distance calculations. The model calculations and anisotropy studies revealed that the donor can nearly be seen as a free rotator allowing the application of the established FRET data evaluation. Topics: Base Sequence; DNA; Fluorescence; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Hydroxyquinolines; Models, Molecular; Oligonucleotides; Organometallic Compounds; Phenanthrolines; Photoelectron Spectroscopy; Quinolones; Spectrometry, Fluorescence	2010

Article

Year

Photophysical characterization of a FRET system using tailor-made DNA oligonucleotide sequences.

Bioconjugate chemistry, 2010, Dec-15, Volume: 21, Issue:12

We have carried out a detailed photophysical study of the FRET D/A pair consisting of a carbostyril donor and a Ru(II)bathophenanthroline complex acceptor in double-stranded synthetic DNA. Altogether 13 different double-stranded 30 base pair DNAs showing small incremental differences in the distances between donor and acceptor were synthesized. Using the fluorescence of the donor as well as of the acceptor, D/A separations were determined and compared to those derived from a well-established model for DNA distance calculations. The model calculations and anisotropy studies revealed that the donor can nearly be seen as a free rotator allowing the application of the established FRET data evaluation.

Topics: Base Sequence; DNA; Fluorescence; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Hydroxyquinolines; Models, Molecular; Oligonucleotides; Organometallic Compounds; Phenanthrolines; Photoelectron Spectroscopy; Quinolones; Spectrometry, Fluorescence

2010