Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Aimée L. Tomlinson"'
Publikováno v:
ACS Omega, Vol 5, Iss 21, Pp 12374-12384 (2020)
Externí odkaz:
https://doaj.org/article/9b6f63909f5e4d4aaab40d658b2a3c96
Autor:
Linda Nhon, Simone L. Tennyson, Mason W. Butt, John Bacsa, Aimée L. Tomlinson, John R. Reynolds
Publikováno v:
Chemistry of Materials. 34:9546-9557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a9b29787f063752df45383780347c33
https://doi.org/10.1021/acs.chemmater.2c02054
https://doi.org/10.1021/acs.chemmater.2c02054
Publikováno v:
Chemistry of Materials. 34:8729-8739
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cdc06dcd6effdb810ec20c20c5cc292
https://doi.org/10.1021/acs.chemmater.2c01884
https://doi.org/10.1021/acs.chemmater.2c01884
Publikováno v:
Macromolecules. 54:1677-1692
Subtle structural changes in monomeric building blocks can have an immense effect, whether positive or detrimental, on the resulting properties of conjugated polymers. With this in mind, it is para...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8a7153c7c8727134e7aa3c8bb506629
https://doi.org/10.1021/acs.macromol.0c02719
https://doi.org/10.1021/acs.macromol.0c02719
Autor:
Jessica Shaw, Volodimyr V. Duzhko, Aimée L. Tomlinson, Malika Jeffries-EL, Alfred A. Burney-Allen, David Wheeler, Lily Diodati
Publikováno v:
Asian Journal of Organic Chemistry. 10:215-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0241bb7cd0c45df17667b54540796e18
https://doi.org/10.1002/ajoc.202000502
https://doi.org/10.1002/ajoc.202000502
Publikováno v:
Chemistry of Materials. 31:6841-6849
A series of conjugated, random terpolymers based on all donor repeat units are prepared via direct (hetero)arylation polymerization yielding cathodically colored electrochromic polymers that span t...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f93c873d2698374b14d31f6a72eb4ec8
https://doi.org/10.1021/acs.chemmater.9b01293
https://doi.org/10.1021/acs.chemmater.9b01293
Publikováno v:
Polymer Chemistry. 9:3055-3066
This study focuses on examining the design principles of creating multi-heterocycle chromophores with a discrete conjugation length, which absorb ultraviolet light in the neutral state and upon oxidation absorb throughout a broad spectral range in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4154d8a5ce1482bf18f647aec29798fa
https://doi.org/10.1039/c8py00385h
https://doi.org/10.1039/c8py00385h
Autor:
Aimée L. Tomlinson, David Wheeler, Malika Jeffries-EL, Ryan S. Gebhardt, Jon Stoffer, Moneim Elshobaki, Benjamin J. Hale, Sumit Chaudhary
Publikováno v:
Polymer. 109:85-92
A donor-acceptor-type conjugated copolymer (PBDT-PPD) composed of benzodithiophene (BDT) and pyrrolopyrroledione (PPD) was synthesized using the Stille cross-coupling reaction. Using both experimental and theoretical data, the optical, electrochemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c4017da0c6d0e62b336dc41b0c13f9e
https://doi.org/10.1016/j.polymer.2016.12.013
https://doi.org/10.1016/j.polymer.2016.12.013
Publikováno v:
Journal of the American Chemical Society. 141(9)
A new paradigm is established for the design of conjugated anodically coloring electrochromic molecules. It is shown that through crossconjugation the electronic energy levels of the radical cation state may be controllably tuned independent of the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d8b31b972331148d50f1a9e38786d2
https://pubmed.ncbi.nlm.nih.gov/30794389
https://pubmed.ncbi.nlm.nih.gov/30794389
Autor:
David Wheeler, Lily Diodati, Jessica Shaw, Malika Jeffries-EL, Aimée L. Tomlinson, Ramiro Chavez
Publikováno v:
The journal of physical chemistry. A. 123(7)
Six 2,4,6,8-tetrarylbenzo[1,2- d:4,5- d']bisoxazoles (BBOs) were synthesized: three bearing phenyl substituents at the 2- and 6-positions and three bearing perfluorophenyl groups at those positions. The influence of perfluoro-aryl group substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d32a511076eb35a1fd2ed66271858e5
https://pubmed.ncbi.nlm.nih.gov/30680993
https://pubmed.ncbi.nlm.nih.gov/30680993