One pot/two donors/one diol give one differentiated trisaccharide: powerful evidence for reciprocal donor–acceptor selectivity (RDAS)

2002 ◽  
pp. 2104-2105 ◽  
Author(s):  
Bert Fraser-Reid ◽  
J. Cristóbal López ◽  
K. V. Radhakrishnan ◽  
M. V. Nandakumar ◽  
Ana M. Gómez ◽  
...  
Keyword(s):  
One Pot ◽  
Donor Acceptor

Metal-Free Photoinduced Hydroalkylation Cascade Enabled by an Electron-Donor-Acceptor Complex

2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  
Keyword(s):  
Electron Donor ◽  
Functional Group ◽  
Photoexcited Electron ◽  
One Pot ◽  
Quaternary Centers ◽  
Metal Free ◽  
Acceptor Complex ◽  
Catalyst Free ◽  
Donor Acceptor ◽  
Radical Cascade

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.

Fluorescent Donor–Acceptor Psoralen Cruciforms by Consecutive Suzuki–Suzuki and Sonogashira–Sonogashira One-Pot Syntheses

2020 ◽  
Vol 85 (15) ◽  
pp. 9737-9750
Author(s):  
Sarah R. Geenen ◽  
Torben Schumann ◽  
Thomas J. J. Müller
Keyword(s):  
One Pot ◽  
Donor Acceptor

ChemInform Abstract: A Convenient Tandem One-Pot Synthesis of Donor-Acceptor-Type Triphenylene 2,3-Dicarboxylic Esters from Diarylacetylene.

ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
Chun Feng ◽  
Xian-Li Tian ◽  
Jing Zhou ◽  
Shi-Kai Xiang ◽  
Wen-Hao Yu ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Donor Acceptor

Facile one-pot polymerization of a fully conjugated donor–acceptor block copolymer and its application in efficient single component polymer solar cells

2019 ◽  
Vol 7 (37) ◽  
pp. 21280-21289 ◽  
Author(s):  
Chang Geun Park ◽  
Su Hong Park ◽  
Youngseo Kim ◽  
Thanh Luan Nguyen ◽  
Han Young Woo ◽  
...  
Keyword(s):  
Solar Cells ◽  
Solar Cell ◽  
Block Copolymer ◽  
Power Conversion Efficiency ◽  
Polymer Solar Cell ◽  
Polymer Solar Cells ◽  
Power Conversion ◽  
Single Component ◽  
One Pot ◽  
Donor Acceptor

A single component polymer solar cell with a CDABP film annealed at 180 °C showed a maximum power conversion efficiency of 5.28%, which is much higher than that (2.62%) of the device with the as-cast film.

A Neutral Donor-Acceptor p-Stack: Solid-State Structures of 1 : 1 Pyromellitic Diimide-Dialkoxynaphthalene Cocrystals

1997 ◽  
Vol 50 (4) ◽  
pp. 271 ◽  
Author(s):  
Rina Carlini ◽  
Cheng-Lin Fang ◽  
Deborah Herrington ◽  
Kerianne Higgs ◽  
Russell Rodrigo ◽  
...  
Keyword(s):  
Solid State ◽  
Diels Alder ◽  
Hypervalent Iodine ◽  
One Pot ◽  
Neutral Donor ◽  
Donor Acceptor ◽  
Solid State Structures

Substituted ortho-benzoquinones, generated in situ by hypervalent iodine oxidation of catechols, are intercepted by unsymmetrical dienes to provide Diels-Alder adducts with complete regiospecificity. Catechols with carboxy substituents in the 3 or 4 positions react similarly and the initial adducts decarboxylate to produce 8-substituted or 5-substituted 1,2-dihydroxydihydronaphthalenes respectively, in a one-pot three-step sequence. The reaction has been further adapted to produce naphtho[1,8-bc]furans in a one-pot process; its application towards the synthesis of the tricyclic system of the sesquiterpene nardonoxide is described

Adducts of Trimeric Perfluro-o-Phenylene Mercury with TTF or DTT

2014 ◽  
Vol 70 (a1) ◽  
pp. C994-C994
Author(s):  
Raul Castaneda ◽  
Sergiu Draguta ◽  
Andrey Yakovenko ◽  
Marina Fonari ◽  
Tatiana Timofeeva
Keyword(s):  
Charge Transfer ◽  
Crystal Growth ◽  
Crystal Shape ◽  
Asymmetric Unit ◽  
Complex Materials ◽  
Slow Evaporation ◽  
One Pot ◽  
Molecular Associates ◽  
Donor Acceptor ◽  
Ct Complex

Since the discovery of metallic conductivity in the TTF-TCNQ complex, the charge transfer (CT) complex materials have been studied for such properties as semiconductivity or superconductivity. The synthesis of new CT materials using trimeric perfluoro-ortho-phenylene mercury (Hg3) as electron acceptor compound was done first by Haneline and Gabaï [1]. A series of studies of CT materials containing Hg3 and tetrathiafulvalene (TTF) or dithieno thiophene (DTT) as an electron donor compounds was carried out by different methods. Co-crystalzation with TTF gave a larger variety of co-crystals than with DTT, producing three polymorphs and one pseudo-polymorph. One pot crystal growth of TTF and Hg3 in a 1:1 mixture of solvents dichloromethane (DCM) and dichloroethane (DCA) has led to the formation of TTF polymorphs 1 and 2 with same 1:1 donor acceptor ratio [Hg3·TTF] as well a pseudopolymorph [Hg3·TTF·DCA] 3 that contains the solvent DCA in the asymmetric unit. Slow evaporation in a 1:1 mixture of dichloromethane and carbon disulfide was used to obtain the previously reported CT [(Hg3)2·TTF] (4)1. By slow evaporation as well in pure dichloromethane was obtained the CT material [Hg3·DTT·DCM] 5. All these five CT co-crystals contain mixed donor acceptor stacks, however only in 3, 4 and 5 these stacks are parallel to each other. In the packing of 1 and 2 these stacks are in herringbone arrangement. Polymorphs 1 and 2 differ in crystal shape and color. Contacts Hg···S shorter than the sum of the Van Der Walls radii were observed in the five CTs materials reported, however only 1, 2, 3, and 5 have extended short donor acceptor molecular associates. Moreover only 3, and 5 has these extended donor acceptor associates along one direction.

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