Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Nathan C. Tice"'
Autor:
Nathan C. Tice, Steven Wild
Publikováno v:
Journal of Molecular Modeling. 27
Polymer and molecular-based electronic materials incorporating heterocycles like thiophenes and pyrroles are attractive possibilities as substitutes for semimetal materials. Heterocyclic materials are heavily studied in this regard due to the large v
Autor:
Eric M. Collins, Darrin L. Smith, Edwin D. Stevens, Nathan C. Tice, Bangbo Yan, Chad A. Snyder
Publikováno v:
Journal of Heterocyclic Chemistry. 54:3235-3240
Oxazine-based chemistry offers an alternative to thiophene and pyrrole semiconductors and has been largely unexplored for electronics applications. Discrete monomers or oxazine polymers could serve as an efficient hole carrier for novel devices. A se
Publikováno v:
Inorganic and Nano-Metal Chemistry. 47:973-977
Furan-based chemistry offers an alternative to thiophene and pyrrole semiconductive materials and has been largely unexplored despite furan's availability from biomass feedstocks. Halogenated furoyl complexes (e.g., 5-bromo) have the potential to be
Autor:
Nathan C. Tice, Benjamin Tyree Cannon, Sarah M. Peak, Sean Parkin, Eli G. Estes, Ethan S. Laha, Chad A. Snyder
Publikováno v:
Journal of Sulfur Chemistry. 35:596-605
A general, convenient route toward N-substituted 5,6-dihydro-4H-thieno[3,4-c]pyrroles was accomplished by the reductive amination of 2,5-dimethylthiophene-3,4-dicarbaldehyde with various primary amines in a solution of sodium cyanoborohydride and met
Autor:
Sana A. Shah, Jesse W. Evans, Chad A. Snyder, B. D. Garabato, Z. A. Claytor, Adam C. Smith, Jason O. E. Young, Levi A. Dopierala, Jeremy B. Maddox, Nathan C. Tice, Michael G. Mazzotta
Publikováno v:
Transition Metal Chemistry. 38:801-809
A series of 5,6-fused ring cyclopentadienyl tricarbonyl manganese and rhenium complexes, [M(CO)3{η 5-1,2-C5H3(1,4-(R)2N2C2}] (2a–3d) were isolated by employing an off-metal ring closure route. Reacting thallium cyclopentadienide (Cp) salts (1a–d
Autor:
Seth L. Sloan, Levi A. Dopierala, Jason O. E. Young, Sana A. Shah, Nathan C. Tice, Michael S. Crocker, Chad A. Snyder, Yuto Kobayashi, Michael G. Mazzotta, Adam C. Smith
Publikováno v:
Synthetic Communications. 43:2441-2451
Thallium cyclopentadiene (Cp) salts are important precursors for the synthesis of a variety of compounds having materials and commercial applications. The synthesis of 5,6-fused ring thallium Cp pyridazines 2a–d from previously reported 5,6-fused r
Autor:
Jason O. E. Young, Nathan C. Tice, Andrew Z. Preston, Daniel F. Hinson, Chad A. Snyder, Marika Wieliczko
Publikováno v:
Transition Metal Chemistry. 37:141-147
A series of 1,2-diacyl cyclopentadienyl tricarbonyl manganese and rhenium complexes, [M(CO)3{η5-1,2-C5H3(CO-(R)2}] (3a–c and 4a–b), were isolated utilizing a straightforward, 3-step route. The synthetic pathway began with a 1,2-diacyl cyclopenta
Autor:
Jeremy B. Maddox, Eric D. Emberton, Nathan C. Tice, Chad A. Snyder, Daniel C. Jackson, Daniel F. Hinson, Eric Vanover
Publikováno v:
Journal of Organometallic Chemistry. 696:2220-2227
The reaction of fulvene 1 with TlOEt in THF affords [Tl{1,2-C5H3(COC4H3O)2}] (2) in 60% yield. Treatment of 2 with [MBr(CO)5] (M = Mn, Re) in benzene reflux gave [Mn{η5-1,2-C5H3(COC4H3O)2}(CO)3] (3A) and [Re{η5-1,2-C5H3(COC4H3O)2}(CO)3] (3B) in 61%
Autor:
Chad L. Phillips, Nilesh Sahi, Phenahas G. Sriramula, Chad A. Snyder, James L. Neathery, Jacob M. Strain, Michael P. Starling, Justin K. Mobley, Nathan C. Tice, Eric Vanover, Andrew Z. Preston
Publikováno v:
Synthetic Communications. 41:1357-1369
Pyridazines are an important class of heterocyclic compounds as a result of their materials and commercial applications. The synthesis of 5,6-fused ring pyridazines 2a–h from 1,2-diacylcyclopentadienes (fulvenes) 1a–h is described herein. This ro
Autor:
Nathan C. Tice, Amber J. Bell, Joseph B. Scott, Paul J. Orosz, Chad A. Snyder, Riley G. Jones, Vineet V. Karambelkar, Jessica M. Wilson
Publikováno v:
Journal of the Kentucky Academy of Science. 70:70-74
An improved route to substituted cyclopenta[c]thiophenes was accomplished by treating 1,3-dimethyl-5,6-dihydro-4H-cyclopenta[c]thiophene-5-one (1) with alkyl Grignard reagents to obtain the 5-alkyl-1,3-dimethyl-4H-cyclopenta[c]thiophenes, 5-methyl-1,