Search results for " Electron Transfer"
showing 10 items of 80 documents
A New ZnIITweezer Pyridine-Naphthalene System - An Off-On-Off System Working in a Biological pH Window
2005
Their basic idea consisted of the connec-tion of an amine to a fluorophoric anthracene unit on oneside and to a pyridine moiety on the other. At acidic pHvalues the amino and the pyridine groups are protonatedand a photoinduced electron transfer (PET) occurs fromthe π-π* excited state of the anthracene to the protonatedpyridinium unit, leading to quenching of the fluorescence.However, at high pH values, where the amino group is notprotonated, PET alternatively takes place from the aminelone pair to the same excited state of the fluorophore, yield-ing the same inhibitory effect on the fluorescence. Betweenthese two pH values, there is a pH window where PET doesnot take place and fluorescence…
Aminoferrocene and Ferrocene Amino Acid as Electron Donors in Modular Porphyrin–Ferrocene and Porphyrin–Ferrocene–Porphyrin Conjugates
2014
New amide-linked porphyrin–ferrocene conjugates [M(PAr)–Fc] were prepared from aminoferrocene and a carboxy-substituted meso-tetraaryl-porphyrin [M = 2H, Zn; Ar = mesityl (Mes), C6F5: 3a, 3e, Zn-3a, Zn-3e]. A further porphyrin building block was attached to the second cyclopentadienyl ring of the ferrocene moiety to give the metallopeptides M(PMes)–Fc–M(PAr) (M = 2H, Zn; Ar = C6H5, 4-C6H4F: 6b, 6c, Zn-6b, Zn-6c). The effects of the Ar substituents, the porphyrin central atom M and the presence of the second porphyrin at the ferrocene hinge on the excited-state dynamics was studied by optical absorption spectroscopy, electrochemistry, steady-state emission, time-resolved fluorescence measure…
Zn(II)-coordination and fluorescence studies of a new polyazamacrocycle incorporating 1H-pyrazole and naphthalene units.
2010
The synthesis and Zn(2+) coordination properties of a new macrocycle (L1) obtained by dipodal (2 + 2) condensation of the polyamine 3-(naphthalen-2-ylmethyl)pentane-1,5-diamine with 1H-pyrazole-3,5-dicarbaldehyde are reported. pH-metric studies show that L1 bears five measurable protonation steps in the 2.0-11.0 pH range. Fluorescence emission studies indicate that the removal of the first proton from the H(5)L1(5+) species leads to a significant decrease in the emission due to a photoinduced electron transfer process. Addition of Zn(2+) promotes a boat-like conformation that approaches both fluorophores and facilitates the formation of an excimer which reaches its highest emission for a 1 …
Thiophene pyrenyl derivatives for the supramolecular processability of single-walled carbon nanotubes in thin film heterojunction
2017
Abstract A major problem for the use of single-wall carbon nanotubes (SWCNTs) in electronic devices relates to their poor processability. Chemical modification inevitably introduces defects in the nanotube lattice, resulting in a loss of electronic properties. In this contest, we report on a supramolecular approach with the aim of increasing the dispersion of SWCNTs in solution and in organic semiconductor matrices by ensuring the optoelectronic properties. In particular, new pyrenyl derivatives of thiophene have been synthesized and used to improve the solubility of SWCNTs for electron transfer in thin film heterojunction with poly(3-hexylthiophene) (P3HT) as donor system. Photoinduced ele…
Grand canonical rate theory for electrochemical and electrocatalytic systems I: General formulation and proton-coupled electron transfer reactions
2020
A generally valid rate theory at fixed potentials is developed to treat electrochemical and electrocatalytic potential-dependent electron, proton, and proton-coupled electron reactions. Both classical and quantum reactions in adiabatic and non-adiabatic limits are treated. The applicability and new information obtained from the theory is demonstrated for the gold catalyzed acidic Volmer reaction.
Enhanced electronic communication through a conjugated bridge in a porphyrin-fullerene donor-acceptor couple
2021
A ZnP-2EDOTV-C60 triad, with enhanced electronic communication between terminus donor and acceptor moieties, was synthesized and studied both experimentally and theoretically. Electrochemical measurements and density functional theory calculations support that the first oxidation takes place on the 3,4-ethylenedioxythiophenevinylene (2EDOTV) bridge followed by the oxidation of the ZnP moiety at slightly higher energies. The electronic communication between the terminal electron-donor ZnP and the electron-acceptor C60 units is enhanced by the conjugated EDOTV-based spacer leading to photoinduced electron transfer over the distance >2 nm in the picosecond time domain. The involvement of the s…
Photoinduced charge transfer from Carbon Dots to Graphene in solid composite
2019
Abstract The emission in solid phase of Carbon Dots (CDs) deposited by drop-casting technique is investigated by means of micro-photoluminescence. Graphene and SiO2 are used as substrates, and the influence of their different nature – conductive or insulating – on the emission of CDs is highlighed. In particular, a systematic loss of efficiency in the emission of CDs on graphene is found, suggesting a CD-graphene interaction possibly due to a photoinduced electron transfer between the surface states of CDs and the conduction band of graphene. Finally, thanks to the negligible influence on CDs emission, SiO2 substrate is used as support to perform thermal processing of CDs in solid phase, sh…
Electrochemical and Spectroelectrochemical Behavior of a Tetracyanotriphenodioxazine in Solution and Thin-Films
2018
International audience; We report the electrochemical behavior of a tetracyano triphenodioxazine bearing two triisopropylsilylethynyl moieties (TiPS‐TPDO‐tetraCN) during its reduction studied either in solution or after vacuum evaporation deposition on indium tin oxide (ITO) support. While in dichloromethane, it typically proceeds in two successive monoelectronic reactions, in acetonitrile, the mechanism appears more complex. Fine analysis of the spectroelectrochemical results combined with simulation of the voltammograms with various amount of water suggest the involvement of water and of a restructured dianion in the electrochemical process. In the solid‐state, the formation of the diprot…
Photoinduced Electron Transfer Reactions in a Porphyrin−Viologen Complex: Observation of S2 to S1 Relaxation and Electron Transfer from the S2 State
1999
Photoinduced Energy Transfer Reactions in a Porphyrin-Viologen Complex: Observation of S2 to S1 Relaxation and Electron Transfer from the S2 state
Dynamic modification of Fermi energy in single-layer graphene by photoinduced electron transfer from carbon dots
2020
Graphene (Gr)&mdash