Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Daniel T. Chase"'
Autor:
Aiden M. Lane, Ny T. C. Luong, Jordan C. Kelly, Martin J. Neal, Jeremiah Jamrom, Aaron J. Bloomfield, Paul A. Lummis, Thomas D. Montgomery, Daniel T. Chase
Publikováno v:
Molecules, Vol 27, Iss 23, p 8256 (2022)
A series of boron, aluminum, gallium, and indium chelates containing the underexplored bis(phenolate) aza-dipyrromethene (aza-DIPY) core were prepared. These compounds were found to possess near-infrared absorption and emission profiles in the 710 to
Externí odkaz:
https://doaj.org/article/5fa197bb7c0742d4aa5a7f84af317718
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 11, Pp 1315-1318 (2015)
Treatment of carbonyl(1,2-diphenylpenta-1,3-dien-1-yl-5-ylidene)bis(triphenylphosphane)iridium, [IrCO(—C(Ph)=C(Ph)—CH=CH—CH=)(PPh3)2], with either bromine or iodine produced dibromido(1,2-diphenylpenta-1,3-dien-1-yl-5-ylidene)(triphenylphosphin
Externí odkaz:
https://doaj.org/article/79390d2cca5c4fec96859281fb1b4f23
Autor:
Samuel R. Zarcone, Hana J. Yarbrough, Martin J. Neal, Jordan C. Kelly, Katie L. Kaczynski, Aaron J. Bloomfield, Geoffrey M. Bowers, Thomas D. Montgomery, Daniel T. Chase
Publikováno v:
New Journal of Chemistry. 46:4483-4496
A series of nitrated aza-BODIPYs on the 2- and 6-positions were regioselectively synthesized and their photophysical properties were examined.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03e10e7da399ac40f58ece95df2b2d8e
https://doi.org/10.1039/d1nj05976a
https://doi.org/10.1039/d1nj05976a
Autor:
Geoffrey M. Bowers, Amanda VerMeulen, Daniel T. Chase, Douglas E. Hovland, Leah R. Eller, Elan Bresslour-Rashap, Andrew S. Koch, Kelly Y. Neiles
Publikováno v:
Journal of Chemical Education. 96:1988-1997
Guiding students to become practicing scientists entails teaching them the specialized ways of collaborating, writing, and thinking that these professionals utilize every day. Laboratory experiences provide unique opportunities for student-centered c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::911f5832971e2ec760573ef8c1ab2e4b
https://doi.org/10.1021/acs.jchemed.9b00008
https://doi.org/10.1021/acs.jchemed.9b00008
Autor:
Jeremy P. Bard, I. David Reingold, Michael M. Haley, Chun-Lin Deng, Wataru Nojo, Daniel T. Chase
Publikováno v:
ChemPlusChem. 84:1391-1395
We have prepared nine structural isomers of a tetrakis(arylethynyl)benzene chromophore functionalized with 4-butoxyphenyl and pyridyl units as the respective donor and acceptor units and examined their steady-state spectroscopic parameters to study h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1cb218088fc0206269af9da301aaff
https://doi.org/10.1002/cplu.201900266
https://doi.org/10.1002/cplu.201900266
Publikováno v:
ACS Symposium Series ISBN: 9780841298668
ACS Symposium Series
ACS Symposium Series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfbe7029fef0ae3b43123c7e046ca6e8
https://doi.org/10.1021/bk-2020-1365.ch008
https://doi.org/10.1021/bk-2020-1365.ch008
Publikováno v:
Organic Letters. 16:812-815
A readily available N,N'-diamidocarbene (DAC) was found to insert into the P-H bonds of primary and secondary phosphines as well as a phosphonate ester. In contrast, tertiary phosphines catalyzed the ring contraction of the DAC to an iminopyrrolidine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d872c1e5be5bad61c337cad8a73aa9
https://doi.org/10.1021/ol4035484
https://doi.org/10.1021/ol4035484
Publikováno v:
Journal of the American Chemical Society. 135:18798-18801
An N,N'-diamidocarbene (DAC) was found to activate a broad range of primary as well as secondary aliphatic and aromatic amines. The relative rates measured for the insertion of the DAC into the primary amines were consistent with an electrophilic act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::029366c8c135192c4b47cb8495425eda
https://doi.org/10.1021/ja411467p
https://doi.org/10.1021/ja411467p
Publikováno v:
The Journal of Organic Chemistry. 76:4043-4051
Six structural isomers of a tetrakis(arylethynyl)benzene (TAEB) chromophore functionalized with dibutylamine and BODIPY moieties as the corresponding donor and acceptor units were prepared. To evaluate the effectiveness of the donor group, two TAEB m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e128c3fa50e708567e3304c726c92201
https://doi.org/10.1021/jo200491m
https://doi.org/10.1021/jo200491m
Publikováno v:
Angewandte Chemie International Edition. 50:1127-1130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d57ae4ecb6a90d9e559edd578597637
https://doi.org/10.1002/anie.201006312
https://doi.org/10.1002/anie.201006312