Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shelby J. Jarrett"'
Publikováno v:
Chemosensors, Vol 11, Iss 3, p 160 (2023)
Push–pull dyes exhibit intramolecular charge transfer behavior, which due to changes in the dipole moment upon excitation, is the origin of their sensitivity to the environment. Such compounds are of interest as probes for bioimaging and as biosens
Externí odkaz:
https://doaj.org/article/9ca2c5fa337445728618f5432561e2e6
Push-pull dyes exhibit intramolecular charge transfer behavior, which due to changes in dipole moment upon excitation, is the origin of their sensitivity to environment. Such compounds are of interest as probes for bioimaging and as biosensors to mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e92c60f9b1e5c479475f67af024e5a0
https://doi.org/10.21203/rs.3.rs-1895397/v2
https://doi.org/10.21203/rs.3.rs-1895397/v2
Autor:
Helena J. Spikes, Shelby J. Jarrett-Noland, Stephan M. Germann, Wendy Olivas, Janet Braddock-Wilking, Cynthia M. Dupureur
Publikováno v:
The 1st International Electronic Conference on Chemical Sensors and Analytical Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4de8818ab15f2dbfc8ca8c1db0937a67
https://doi.org/10.3390/csac2021-10455
https://doi.org/10.3390/csac2021-10455
Autor:
Janet Braddock-Wilking, Shelby J. Jarrett-Noland, Stephan Germann, Helena J. Spikes, Cynthia M. Dupureur
Sila- and germafluorenes containing alkynyl(aryl) substituents at the 2,7- position are strongly emissive with high quantum yields in organic solvents. Provided they are sufficiently soluble in water, their hydrophobic structures have the potential f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2612eafdb6bdd012b9443864375ca82d
https://doi.org/10.21203/rs.3.rs-260292/v1
https://doi.org/10.21203/rs.3.rs-260292/v1
Autor:
Helena J, Spikes, Shelby J, Jarrett-Noland, Stephan M, Germann, Janet, Braddock-Wilking, Cynthia M, Dupureur
Publikováno v:
Journal of fluorescence. 31(4)
Sila- and germafluorenes containing alkynyl(aryl) substituents at the 2,7- position are strongly emissive with high quantum yields in organic solvents. Provided they are sufficiently soluble in water, their hydrophobic structures have the potential f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c8c17c1a63eb91c4cbb36ad26493114
https://pubmed.ncbi.nlm.nih.gov/33821437
https://pubmed.ncbi.nlm.nih.gov/33821437
Autor:
Janet Braddock-Wilking, Shelby J. Jarrett, Ethan Gallaher, Cynthia M. Dupureur, Stephan Germann, Nigam P. Rath
Publikováno v:
Journal of Organometallic Chemistry. 927:121514
Three new fluorescent 2,7-alkynyl(aryl)-3,6-dimethoxy-9,9-diphenylsilafluorenes have been synthesized using a Pd-catalyzed Sonogashira coupling reaction to incorporate alkynyl(aryl) groups at the 2,7-positions of the ring. The substituents include 9-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69ec09b098e6931ee5541a5c2917fdc1
https://doi.org/10.1016/j.jorganchem.2020.121514
https://doi.org/10.1016/j.jorganchem.2020.121514