scholarly journals Synthesis and Characterization of Four Random copolymers Containing Fluorene as Electron Donors and Benzotriazole, Benzothiadiazole, Pyrido[3,4-b]pyrazine as Electron Acceptors

Author(s):  
Shuang Chen ◽  
2006 ◽  
Vol 2006 (18) ◽  
pp. 4237-4241 ◽  
Author(s):  
Noura Benbellat ◽  
Yann Le Gal ◽  
Stéphane Golhen ◽  
Abdelkrim Gouasmia ◽  
Lahcène Ouahab ◽  
...  

2016 ◽  
Vol 180 ◽  
pp. 170-174 ◽  
Author(s):  
Hohyoun Jang ◽  
Hyunho Joo ◽  
Sabuj Chandra Sutradhar ◽  
Nipa Banik ◽  
Jaeseong Ha ◽  
...  

1992 ◽  
Vol 114 (14) ◽  
pp. 5708-5713 ◽  
Author(s):  
Vincenzo G. Albano ◽  
Loris Grossi ◽  
Giuliano Longoni ◽  
Magda Monari ◽  
Suzanne Mulley ◽  
...  

2006 ◽  
Vol 71 (4) ◽  
pp. 1351-1361 ◽  
Author(s):  
Christophe Desmarets ◽  
Benoît Champagne ◽  
Alain Walcarius ◽  
Christine Bellouard ◽  
Rafik Omar-Amrani ◽  
...  

1996 ◽  
Vol 74 (11) ◽  
pp. 2378-2385 ◽  
Author(s):  
Jin Li ◽  
Kattesh V. Katti ◽  
Ronald G. Cavell ◽  
A. Alan Pinkerton ◽  
Herbert Nar

Reaction of tetrafluoro- or tetrachloro-p-benzoquinone with silylated phosphoranimines R2R′P=NSiMe3 (R = Ph, Me) yields very highly colored monosubstituted derivatives of the p-quinone that act as two-electron acceptors showing clean, reversible CV traces. The molar absorptivity values are typical of dyes. These ligands also form chelate complexes with Rh(I) precursors using the quinone oxygen and the imine nitrogen donor sites. One of the quinone derivatives, 3,5,6-trichloro-2-(triphenylphosphinimino)-p-benzoquinone, has been structurally characterized. The iminated quinone shows a normal P=N bond length (1.597(2) Å) and P-N-C angle (P-N-C(3) 132.7(2)°). The N—C(3) bond, 1.327(3) Å, is a little shorter as is expected for the establishment of a conjugated structure between the phosphinimine substituent and the quinone ring. Some steric crowding pushes the Cl and N substituents on the quinone ring out of the plane of the ring. Key words: quinones, phosphinimines, fluorine, chlorine, rhodium.


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