Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hayden T. Black"'
Autor:
Hayden T. Black, Mathias C. Celina, Brad H. Jones, Nicholas Henry Giron, Todd M. Alam, Timothy N. Lambert, Mark E. Stavig, Patricia Sue. Sawyer, David R. Wheeler
Publikováno v:
Macromolecules. 50:5014-5024
Physical stress relaxation in rubbery, thermoset polymers is limited by cross-links, which impede segmental motion and restrict relaxation to network defects, such as chain ends. In parallel, the cure shrinkage associated with thermoset polymerizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a711ea41e3cdc1e9d3d97bee26be3960
https://doi.org/10.1021/acs.macromol.7b00501
https://doi.org/10.1021/acs.macromol.7b00501
Publikováno v:
Chemistry - A European Journal. 22:17251-17261
A comprehensive investigation of the complementary H-bonding-mediated self-assembly between dipyrrolo[2,3-b:3',2'-e]pyridine (P2P) electron donors and naphthalenediimide/perylenediimide (NDI/PDI) acceptors is reported. The synthesis of parent P2P and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bddaaf9173b184caf4fb5834232fac2
https://doi.org/10.1002/chem.201602543
https://doi.org/10.1002/chem.201602543
Publikováno v:
Organic Letters. 17:4224-4227
Two new contorted polycyclic aromatic hydrocarbons (PAHs) 1 and 2 were synthesized by acid-catalyzed benzannulation of a substituted anthracene. The isomers reveal dissimilar photophysical and redox properties with 2 having a much smaller HOMO-LUMO g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6afc455f4fe8626ab2eff78bddf53cd2
https://doi.org/10.1021/acs.orglett.5b02009
https://doi.org/10.1021/acs.orglett.5b02009
Autor:
Dmitrii F. Perepichka, Hayden T. Black
Publikováno v:
Angewandte Chemie. 126:2170-2174
The supramolecular arrangement of organic semiconductors in the solid state is as critical for their device properties as the molecular structure, but is much more difficult to control. To enable supramolecular design of semiconducting materials, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefeebdc20c69bb496809f596b0cfe06
https://doi.org/10.1002/ange.201310902
https://doi.org/10.1002/ange.201310902
Publikováno v:
J. Mater. Chem. C. 1:260-267
A series of oligothiophenes containing either electron withdrawing perfluorohexyl substituents or an electron deficient benzothiadiazole core, or both, were synthesized and their properties were evaluated by optical spectroscopy, cyclic voltammetry a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed92d84b198729b9b52072da81e7c4d8
https://doi.org/10.1039/c2tc00032f
https://doi.org/10.1039/c2tc00032f
Autor:
Katharine L. Harrison, Hayden T. Black
The synthesis and characterization of the first polyelectrolyte of intrinsic microporosity (PEIM) is described. The novel material was synthesized via reaction between the nitrile group in the polymer backbone and n-butyl lithium, effectively anchori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9822dc10612cdfe6777b7733538395c
https://doi.org/10.2172/1330204
https://doi.org/10.2172/1330204
Publikováno v:
Organic Letters. 13:6492-6495
Two fused thienoacene compounds with two-dimensional ring connectivity were synthesized, and their semiconducting properties were characterized. Both compounds have a crystal structure comprised of herringbone arrays of tight π-π stacks. Strong π-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bbe906aa8b4656ee6b4c33dd245c2e4
https://doi.org/10.1021/ol202662s
https://doi.org/10.1021/ol202662s
Publikováno v:
The Journal of Organic Chemistry. 79:5858-5860
A new heteroacenequinone, pentaceno[2,3-c:9,10-c']bis([1,2,5]thiadiazole)-6,13-dione (PBTDQ), with two peripheral thiadiazole rings was synthesized, and its solid-state properties were characterized. The fused planar structure with a low-lying LUMO a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e94afc9360c0855676bb9c17dba567
https://doi.org/10.1021/jo500760c
https://doi.org/10.1021/jo500760c