Search results for "Electron acceptor"
showing 10 items of 83 documents
Fumarate respiration of Wolinella succinogenes: enzymology, energetics and coupling mechanism.
2002
Wolinella succinogenes performs oxidative phosphorylation with fumarate instead of O2 as terminal electron acceptor and H2 or formate as electron donors. Fumarate reduction by these donors ('fumarate respiration') is catalyzed by an electron transport chain in the bacterial membrane, and is coupled to the generation of an electrochemical proton potential (Deltap) across the bacterial membrane. The experimental evidence concerning the electron transport and its coupling to Deltap generation is reviewed in this article. The electron transport chain consists of fumarate reductase, menaquinone (MK) and either hydrogenase or formate dehydrogenase. Measurements indicate that the Deltap is generat…
1,2,3,4,5‐[1′,8′] Anthra‐8,9;10,11‐dibenzo[13]annulene and 1,8‐Distyrylanthracene as Models for Phenylenevinylene Species. Syntheses, Structures, and…
1987
The synthesis of the title compound 4, formally a [13] perimeter, and of its acyclic model system, 1,8-distyrylanthracene (6) is described. The crystal structure of 4 reveals the configuration of the double bonds and the conformation of the macrocycle. Related findings come from the 1H-NMR spectroscopic characterization of 4 and 6 in solution. The spin density distribution of the radical anions 4−· and 6−· is interpretet in terms of the singly occupied molecular orbital and of the prevailing geometry. In contrast to 4, compund 6 proves to be an efficient electron acceptor since it can even be reduced to a tetraanion salt. The complete redox sequence is characterized by NMR and ESR spectrosc…
Tuning Reductive and Oxidative Photoinduced Electron Transfer in Amide‐Linked Anthraquinone–Porphyrin–Ferrocene Architectures
2014
Porphyrin amino acids 3a–3h with meso substituents Ar of tunable electron-donating power (Ar = 4-C6H4OnBu, 4-C6H4OMe, 4-C6H4Me, Mes, C6H5, 4-C6H4F, 4-C6H4CF3, C6F5) have been linked at the N terminus to anthraquinone Q as electron acceptor through amide bonds to give Q-PAr dyads 4a–4h. These were conjugated to ferrocene Fc at the C terminus as electron donor to give the acceptor-chromophore-donor Q-PAr-Fc triads 6a–6h. To further modify the energies of the electronically excited and charge-separated states, the triads 6a–6h were metallated with zinc(II) to give the corresponding Q-(Zn)PAr-Fc triads Zn-6a–Zn-6h. The Q-PAr1 dyad (Ar1 = C6H5) was further extended with a second porphyrin PAr2 (…
Au70S20(PPh3)12: an intermediate sized metalloid gold cluster stabilized by the Au4S4 ring motif and Au-PPh3 groups
2018
Reducing (Ph3P)AuSC(SiMe3)3 with L-Selectride® gives the medium-sized metalloid gold cluster Au70S20(PPh3)12. Computational studies show that the phosphine bound Au-atoms not only stabilize the electronic structure of Au70S20(PPh3)12, but also behave as electron acceptors leading to auride-like gold atoms on the exterior.
Light-induced charge separation in a donor–chromophore–acceptor nanocomposite poly[TPA-Ru(tpy)2]@ZnO
2013
The synthesis and characterisation of a new donor–chromophore–acceptor system based on poly(vinyltriphenylamine) as the electron donor and a glycine-functionalised bis(2,2′;6′,2′′-terpyridine)ruthenium(II) complex acting both as a chromophore and as an anchor group attached to ZnO nanorods as the electron acceptor are described. The TPA-containing block copolymer was synthesised by Reversible Addition Fragmentation Chain Transfer (RAFT) polymerisation and the ruthenium complex glycine conjugates prepared by Solid Phase Peptide Synthesis (SPPS) were attached via post-polymerisation esterification. GPC, NMR, IR and UV-Visible spectroscopy were used to characterise the multifunctional chromoph…
A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer
2017
International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…
A Novel Gas Sensor Transducer Based on Phthalocyanine Heterojunction Devices
2007
Abstract: Experimental data concerning the changes in the current-voltage (I-V) perfor-mances of a molecular material-based heterojunction consisting of hexadecafluorinated nickel phthalocyanine (Ni(F 16 Pc)) and nickel phthalocyanine (NiPc), (Au|Ni(F 16 Pc)|NiPc|Al) are introduced as an unprecedented principle of transduction for gas sensing performances. The respective n - and p -type doped-insulator behaviors of the respective materials are supported, owing to the observed changes in surface potential (using the Kelvin probe method) after submission to electron donor (ammonia) and electron acceptor gases (ozone). On the other hand, the bilayer device exhibits strong variations in the bui…
Tetrathiafulvalene-Polychlorotriphenylmethyl Dyads: Influence of Bridge and Open-Shell Characteristics on Linear and Nonlinear Optical Properties
2017
Three conjugated donor-π-acceptor radical systems (1 a–1 c) were prepared by bridging a tetrathiafulvalene (TTF) electron-donor unit to a polychlorotriphenylmethyl (PTM) electron-acceptor radical through vinylene units of different lengths. The dependence of the intramolecular charge transfer on the length of the conjugated bridge has been analyzed by different electrochemical and spectroscopic techniques. Linear optical properties and the second-order nonlinear optical (NLO) response of these derivatives have been computed by comparing systems 1 a–1 c with the non-radical analogues (2 a–2 c). Interestingly, an enhanced NLO response is predicted for dyads 1 a–1 c with PTM in the radical for…
Bis-Sulfone- and Bis-Sulfoxide-Spirobifluorenes: Polar Acceptor Hosts with Tunable Solubilities for Blue-Phosphorescent Light-Emitting Devices
2016
Bis-sulfone- and bis-sulfoxide-spirobifluorenes are a promising class of high-triplet-energy electron-acceptor hosts for blue phosphorescent light-emitting devices. The molecular design and synthetic route are simple and facilitate tailoring of the solubilities of the host materials without lowering the high-energy triplet state. The syntheses and characterization (including single-crystal structures) of four electron-accepting hosts are reported; the trend in their reduction potentials is consistent with the electron-withdrawing nature of the sulfone or sulfoxide substituents. Emission maxima of 421–432 nm overlap with the MLCT absorption of the sky-blue emitter bis(4,6-difluorophenyl-pyri…
PV and magnetic field effects in poly(3-hexylthiophene)-fullerene cells doped with phthalocyanine soluble derivative
2007
An attempt was made to widen the photosensitivity spectral range of poly(3-hexylthiophene)-fullerene blend by adding an extra electron donor — a newly synthesized soluble phthalocyanine derivative (SnClPc) having the electron absorption band at 708 nm. As the electron acceptor, home-synthesised di(ethoxycarbonyl) methano-fullerene carboxylate (C 61 (CO 2 Et) 2 ) was used, and as the hole transporter — the regioregular poly 3-hexylthiophene (P3HT). The sandwich-type samples were prepared on an ITO glass substrate by coating it with a 30–50 nm thick PEDOT:PSS layer followed by a ~100 nm thick P3HT:C 61 (CO 2 Et) 2 :SnClPc blend. For the top electrodes In or Au were used. Spectral dependences …