Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Alexander K. Lay"'
Autor:
Maria S. Galletero, Hermenegildo García, Mercedes Alvaro, Alexander K. Lay, Carlos J. Gómez-García
Publikováno v:
Physical Chemistry Chemical Physics. 4:115-120
Upon polymerisation of acetylene and propyne inside the channels of Ni2+-exchanged mordenite and mesoporous MCM-41 spontaneous doping and formation of antiferromagnetic NiO clusters are observed to various extents. The population of polarons present
Autor:
Pascal Merstetter, Antony Chesney, Fabian Gerson, Andrei S. Batsanov, Martin R. Bryce, Alexander K. Lay, Urs Buser, Judith A. K. Howard
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :755-764
Syntheses of acenaphtho[1,2-b][1,4]oxathiine 4 and 8,9-bis(methylsulfanyl)acenaphtho[1,2-b][1,4]dithiine 5 are reported. The fairly persistent radical ions of acenaphtho[1,2-b][1,4]dithiine 1, acenaphtho[1,2-b][1,4]benzodithiine 2, acenaphtho[1,2-b]t
Publikováno v:
Tetrahedron Letters. 40:801-804
The reaction of transient 1,3-dithiole-2,4,5-trithione 4 with acenaphthylene afforded the Diels-Alder adduct 5, which was dehydrogenated to yield 6; cross-coupling of 6 with 7 gave the tetrathiafulvalene (TTF) derivative 8, which was converted into t
Autor:
Alexander K. Lay, L. Binet, Judith A. K. Howard, Antony Chesney, Jean-Marc Fabre, Martin R. Bryce, Azarang Javidan, Andrew Green, Andrei S. Batsanov, Shimon Yoshida
Publikováno v:
Tetrahedron. 54:13257-13266
The synthesis is described of a series of conjugated donor-π-acceptor molecules where 1,3-diselenoles are the electron donor moieties and dicyanomethylene or N-cyanoimine groups function as the acceptor moieties. Alkenes and aryl groups act as the c
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2451-2459
Syntheses of the acenaphtho[1,2-b][1,4]dithiine derivatives 12, 25 and 29 are reported. Cyclic voltammetric studies reveal that these compounds undergo reversible single-electron oxidations at < 1.0 V, vs. Ag/AgCl. Lithiation of compound 12 with BuLi
Publikováno v:
ChemInform. 28
Syntheses of the acenaphtho[1,2-b][1,4]dithiine derivatives 12, 25 and 29 are reported. Cyclic voltammetric studies reveal that these compounds undergo reversible single-electron oxidations at < 1.0 V, vs. Ag/AgCl. Lithiation of compound 12 with BuLi
Autor:
Andrei S. Batsanov, Shimon Yoshida, Antony Chesney, L. Binet, Azarang Javidan, Alexander K. Lay, Jean-Marc Fabre, Martin R. Bryce, Judith A. K. Howard, Andrew Green
Publikováno v:
ChemInform. 30
The synthesis is described of a series of conjugated donor-π-acceptor molecules where 1,3-diselenoles are the electron donor moieties and dicyanomethylene or N-cyanoimine groups function as the acceptor moieties. Alkenes and aryl groups act as the c
Publikováno v:
ChemInform. 30
Photolysis of 1,2-dithiole-3-thione derivative 1 results in the formation of the 1,2,4-trithiolane derivative 2, the structure of which was established by single crystal X-ray analysis. Interesting bond delocalisation is observed in the molecular str
Publikováno v:
Journal of Heterocyclic Chemistry. 36:823-825
Photolysis of 1,2-dithiole-3-thione derivative 1 results in the formation of the 1,2,4-trithiolane derivative 2, the structure of which was established by single crystal X-ray analysis. Interesting bond delocalisation is observed in the molecular str
Publikováno v:
Journal of Materials Chemistry; Jan2005, Vol. 15 Issue 3, p403-406, 4p