1380077-15-5Relevant academic research and scientific papers
ANALYTE DETECTION USING NEAR-INFRARED FLUOROPHORES
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Paragraph 0174, (2016/08/29)
Embodiments of compounds for selectively detecting an analyte are disclosed, along with methods and kits for detecting analytes with the compounds. The compounds are bridged viologen conjugates including at least one fluorophore according to the general structure At least one of R1/R2, R2/R3, R3/R4, R5/R6, R6/R7, and/or R7/R8 together form a substituted or unsubstituted cycloalkyl or aryl.
Near-infrared fluorescent dyes with large stokes shifts
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Page/Page column 42-43, (2016/02/26)
Embodiments of near-infrared (NIR) dyes are disclosed, along with methods and kits for detecting analytes with the NIR dyes. The NIR dyes have a structure according to the general structure At least one of R1/R2, R2/R3, R3/R4, R5/R6, R6/R7, and/or R7/R8 together forms a substituted or unsubstituted cycloalkyl or aryl.
Field effects induce bathochromic shifts in xanthene dyes
Sibrian-Vazquez, Martha,Escobedo, Jorge O.,Lowry, Mark,Fronczek, Frank R.,Strongin, Robert M.
supporting information; experimental part, p. 10502 - 10508 (2012/08/08)
There is ongoing interest in near-infrared (NIR) absorbing and emitting dyes for a variety of biomedical and materials applications. Simple and efficient synthetic procedures enable the judicious tuning of through-space polar (field) effects as well as low barrier hydrogen bonding to modulate the HOMO-LUMO gap in xanthene dyes. This affords unique NIR-absorbing xanthene chromophores.
