Magnetic properties of a charge transfer compound of electron-acceptor moiety [CoL2] and 5, 10-dimethyl-dihydrophenazine

Author(s):  
R. T. Pardasani ◽  
P. Pardasani
2006 ◽  
Vol 398 (1) ◽  
pp. 113-124 ◽  
Author(s):  
Hana Popelková ◽  
Marco W. Fraaije ◽  
Ondřej Novák ◽  
Jitka Frébortová ◽  
Kristin D. Bilyeu ◽  
...  

CKX (cytokinin dehydrogenase) is a flavoprotein that cleaves cytokinins to adenine and the corresponding side-chain aldehyde using a quinone-type electron acceptor. In the present study, reactions of maize (Zea mays) CKX with five different substrates (N6-isopentenyladenine, trans-zeatin, kinetin, p-topolin and N-methyl-isopentenyladenine) were studied. By using stopped-flow analysis of the reductive half-reaction, spectral intermediates were observed indicative of the transient formation of a binary enzyme–product complex between the cytokinin imine and the reduced enzyme. The reduction rate was high for isoprenoid cytokinins that showed formation of a charge-transfer complex of reduced enzyme with bound cytokinin imine. For the other cytokinins, flavin reduction was slow and no charge-transfer intermediates were observed. The binary complex of reduced enzyme and imine product intermediate decays relatively slowly to form an unbound product, cytokinin imine, which accumulates in the reaction mixture. The imine product only very slowly hydrolyses to adenine and an aldehyde derived from the cytokinin N6 side-chain. Mixing of the substrate-reduced enzyme with Cu2+/imidazole as an electron acceptor to monitor the oxidative half-reaction revealed a high rate of electron transfer for this type of electron acceptor when using N6-isopentenyladenine. The stability of the cytokinin imine products allowed their fragmentation analysis and structure assessment by Q-TOF (quadrupole–time-of-flight) MS/MS. Correlations of the kinetic data with the known crystal structure are discussed for reactions with different cytokinins.


2015 ◽  
Vol 16 (8) ◽  
pp. 1605-1610 ◽  
Author(s):  
Seon-Yeong Gwon ◽  
Satheshkumar Angupillai ◽  
Young-A Son ◽  
Sung-Hoon Kim

IUCrData ◽  
2018 ◽  
Vol 3 (1) ◽  
Author(s):  
Takuya Fujii ◽  
Hideo Yamakado

The title compound, 2C14H12S·C12N4F4, was obtained by using 4,6-dimethyldibenzothiophene (DMDBT) as an electron donor and 7,7,8,8-tetracyano-2,3,5,6-tetrafluoroquinodimethane (F4TCNQ) as an electron acceptor. The asymmetric unit consists of one DMDBT molecule and one half of an F4TCNQ molecule, which lies on an inversion centre. In the crystal, the DMDBT and F4TCNQ molecules form a 2:1 unit via a charge-transfer interaction, with a centroid–centroid distance of 3.3681 (15) Å between the five-membered ring of DMDBT and the six-membered ring of F4TCNQ. An F...F contact [2.911 (1) Å] is also observed.


2003 ◽  
Vol 771 ◽  
Author(s):  
Vladimir I. Arkhipov ◽  
Paul Heremans ◽  
Evgenia V. Emelianova ◽  
Heinz Bässler

AbstractA model of carrier photogeneration in doped conjugated polymers is formulated. The model suggests that dissociation of a relaxed exciton into a Coulombically bound geminate pair (GP) occurs at a charge transfer center that consists of a polymer chain and a nearby electron acceptor. Further dissociation of the GP into free carriers is facilitated either by the kinetic energy of the zero-point oscillation of the on-chain carrier at low dopant concentrations or by the interfacial potential barrier for geminate pair recombination in polymer/electron acceptor blends.


2017 ◽  
Vol 73 (6) ◽  
pp. 476-480 ◽  
Author(s):  
Rikako Tanaka ◽  
Nobuyuki Matsushita

The methyl viologen dication, used under the name Paraquat as an agricultural reagent, is a well-known electron-acceptor species that can participate in charge-transfer (CT) interactions. The determination of the crystal structure of this species is important for accessing the CT interaction and CT-based properties. The title hydrated salt, bis(1,1′-dimethyl-4,4′-bipyridine-1,1′-diium) hexacyanidoferrate(II) octahydrate, (C12H14N2)2[Fe(CN)6]·8H2O or (MV)2[Fe(CN)6]·8H2O [MV2+ is the 1,1′-dimethyl-4,4′-bipyridine-1,1′-diium (methyl viologen) dication], crystallizes in the space group P21/c with one MV2+ cation, half of an [Fe(CN)6]4− anion and four water molecules in the asymmetric unit. The FeII atom of the [Fe(CN)6]4− anion lies on an inversion centre and has an octahedral coordination sphere defined by six cyanide ligands. The MV2+ cation is located on a general position and adopts a noncoplanar structure, with a dihedral angle of 40.32 (7)° between the planes of the pyridine rings. In the crystal, layers of electron-donor [Fe(CN)6]4− anions and layers of electron-acceptor MV2+ cations are formed and are stacked in an alternating manner parallel to the direction of the −2a + c axis, resulting in an alternate layered structure.


1997 ◽  
Vol 90 (3) ◽  
pp. 407-413
Author(s):  
MARC KELEMEN ◽  
CHRISTOPH WACHTER ◽  
HUBERT WINTER ◽  
ELMAR DORMANN ◽  
RUDOLF GOMPPER ◽  
...  

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