Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mitchell Denti"'
Publikováno v:
US20170237042A1, Internazionale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::11bc8679217aaa7a2efc24d93d934c9e
http://www.cnr.it/prodotto/i/393323
http://www.cnr.it/prodotto/i/393323
Publikováno v:
Tetrahedron Letters. 55:4501-4504
Upon utilization of some common methods described in the literature for the synthesis of chiral, 2-substituted 2,5-diketopiperazines, extensive racemization was observed. Further investigation showed that heating in the presence of a mild base racemi
Autor:
Hakan Usta, Alyssa-Jennifer Avestro, Antonio Facchetti, Mitchell Denti, Wei Zhao, Damien Boudinet, M. Deniz Yilmaz, J. Fraser Stoddart
Publikováno v:
Advanced Materials. 25:4327-4334
The synthesis and physicochemical properties of a new class of BODIPY-based donor-acceptor π-conjugated polymers are presented. Solution-processed top-gate/bottom-contact (TG-BC) thin-film transistors on flexible plastic substrates exhibit air-stabl
Autor:
Tejender S. Thakur, Sudhir Kumar Keshri, Antonio Facchetti, Yogendra Kumar, Mitchell Denti, Jyoti Shukla, Sharvan Kumar, Shiv Shankar Singh, Pritam Mukhopadhyay
Publikováno v:
Organic letters. 18(3)
A facile synthesis of octabromoperylene-3,4,9,10-tetracarboxylic dianhydride (Br8-PDA) (1), its diimides (Br8-PDIs) (2a-e), and bis-, tris-, and tetra-amino substituted diimides (5a-c) with six, five, and four remaining substitutable Br atoms, respec
Autor:
Fausta Loffredo, Antonio Facchetti, Riccardo Miscioscia, Mario Petrosino, Giuseppe Nenna, Carla Minarini, Fulvia Villani, Alfredo Rubino, Mitchell Denti
The variations in physical parameters of an organic field-effect transistor having dioctylbenzothieno[2,3-b]benzothiophene (C8BTBT) as the channel semiconductor were investigated under different light irradiation conditions at wavelengths of 350 nm,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff90718a7291c4b37db6aad92b29f4c7
http://www.scopus.com/inward/record.url?eid=2-s2.0-84955595249&partnerID=40&md5=d6b62e76b018db54aa28e9cf6182ebdc
http://www.scopus.com/inward/record.url?eid=2-s2.0-84955595249&partnerID=40&md5=d6b62e76b018db54aa28e9cf6182ebdc
Publikováno v:
EP 2 978 035 A1, Europeo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::360e7f859dab3c5823bce76cc44d47c5
http://www.cnr.it/prodotto/i/393319
http://www.cnr.it/prodotto/i/393319
Publikováno v:
ChemInform. 46
Upon utilization of some common methods described in the literature for the synthesis of chiral, 2-substituted 2,5-diketopiperazines, extensive racemization was observed. Further investigation showed that heating in the presence of a mild base racemi
Autor:
Michele Muccini, Gianluca Generali, Shaofeng Lu, Xinge Yu, Raffaella Capelli, Hakan Usta, Antonio Facchetti, Mitchell Denti, William C. Sheets
Publikováno v:
Chemistry of materials 26 (2014): 6542–6556. doi:10.1021/cm503203w
info:cnr-pdr/source/autori:Usta, Hakan; Sheets, William Christopher; Denti, Mitchell; Generali, Gianluca; Capelli, Raffaella; Lu, Shaofeng; Yu, Xinge; Muccini, Michele; Facchetti, Antonio/titolo:Perfluoroalkyl-Functionalized Thiazole Thiophene Oligomers as N-Channel Semiconductors in Organic Field-Effect and Light-Emitting Transistors/doi:10.1021%2Fcm503203w/rivista:Chemistry of materials/anno:2014/pagina_da:6542/pagina_a:6556/intervallo_pagine:6542–6556/volume:26
info:cnr-pdr/source/autori:Usta, Hakan; Sheets, William Christopher; Denti, Mitchell; Generali, Gianluca; Capelli, Raffaella; Lu, Shaofeng; Yu, Xinge; Muccini, Michele; Facchetti, Antonio/titolo:Perfluoroalkyl-Functionalized Thiazole Thiophene Oligomers as N-Channel Semiconductors in Organic Field-Effect and Light-Emitting Transistors/doi:10.1021%2Fcm503203w/rivista:Chemistry of materials/anno:2014/pagina_da:6542/pagina_a:6556/intervallo_pagine:6542–6556/volume:26
Despite their favorable electronic and structural properties, the synthetic development and incorporation of thiazole-based building blocks into n-type semiconductors has lagged behind that of other pi-deficient building blocks. Since thiazole insert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64fd49c4739e8b9946dec14840c227f
https://publications.cnr.it/doc/320053
https://publications.cnr.it/doc/320053