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Electron Transfer Through Dendrimers in Solution. Deborah Evans. University of New Mexico. Department of Chemistry and the Albuquerque High Performance Computing Center. Dendrimers are synthetic realizations of Caley trees:. Electron Transfer:. Energy Transfer:.
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Electron Transfer Through Dendrimers in Solution Deborah Evans University of New Mexico Department of Chemistry and the Albuquerque High Performance Computing Center
Dendrimers are synthetic realizations of Caley trees: Electron Transfer: Energy Transfer:
Electron Transfer Through Dendrimers: • Extensively branched macromolecules Crooks et al, JACS, 120 (1998) • form self-assembled monolayers Abruna and coworkers Langmuir, 15 (1999)
Electro-active dendrimers and encapsulation Cores: Fe-S, porphyrin, ferrocene: Gorman et al, JACS, 121 (1999)
STM and cyclic voltammetry Gorman et al JACS, 121 (1999)
Electron Transfer and Molecular Electronics: It's All About Contacts K.W. Hipps, Science The goal of building sophisticated electronic devices from individual molecules has spurred studies of single-molecules. The primary problems facing the molecular electronics designer are: measuring and predicting electron transport. • Molecular “wires”: Molecular break-junction experiments Reed et al JACS, 121 (1999)
Electron transport through linear chains: Nitzan et al, JPC, 104, 2001 bridge electron transfer: interferences and solvent dephasing Pollard and Friesner, JPC, 99, 1995
ET through solvated branched molecules • Photo-induced intra-molecular transfer Wasielewski et al JACS, 121 (1999)
Simulation of ET in solvated dendrimers: Experiments have many competing processes: • Intra-dendrimer transfer • solvent-induced relaxation / diffusion • surface effects • Surface-induced distortions Crooks et al, Anal. Chem. , 71 (1999)
Donors or Acceptors in solution: • D/A superexchange
Previous Modeling Extended systems: • infinite Caley trees • localized states • dimensionality (simply connected; branching) Electron Transfer Pathways: Electron transfer rate: |T|2 ~ 1 / K K Disorder: creates 1-D pathways to enhance rate Beratan, Onuchic, 1994
Solvent effects on ET • Solvent-dependent ET rates • flexible hydrophobic/hydrophilic • rigid dendrimers: Classical MC and MD studies of 1-4 generations: Newhouse, Evans, 2000. kJ/mol
Simulation of condensed phase ET • Split-operator methods : • Time-dependent simulation of photo- induced electron transfer • Solvent influence included as time- dependent fluctuations in the Hamiltonian A modified Checkerboard algorithm exploits the Caley tree connectivity
Phenomenological Density MatrixApproach : • Liouville density matrix equation of motion: • Solvent influence included as phenomenological decay rates • Steady-state rate constants determined for effective electron transfer rates through the molecular wire [Ratner, Nitzan et al, linear D-B-A]
Redfield Approach : • Approach used formulti-level electron transfer • Solvent included in the Redfield tensor elements Rijkl • Bath correlation functions taken from the high- temperature limit • Reduced density matrix of the system propagated using a symplectic integrator scheme:
Numerical Techniques : Photo-induced experiments (population dynamics): Steady-State (rates): : constant
Solvated Dendrimer models: • Tight-binding model for dendrimer: • D E ~ 1000 ; b ~ 100 • Solvent – system coupling • coupling strength ~ 5-10 • Assume Markovian limit
Results from numerical simulations: Effects of: • Dendrimer topology/geometry • Solvent-induced relaxation • Donor/acceptor energies • Side-branch chemistry • Thermal relaxation of the bridge On: • electron transfer rates • rectification • switching • conductance
Photo-induced Electron Transfer (3N) (4N) (5N) condensed dendrimers (14) (33) (52) extended dendrimers
Steady-state rates: Dendrimer bridges vs linear chains Evans et al , JPC, 2001 dendrimer linear
Forward Backward
Electronic Effects in Molecular Wires: molecule between two metal contacts: Conductance ( |G(V)|2) vs voltage (units of Eb)
Bridge Topology and Conductance linear chains side-branch structure side-branch position
number of side-branches longer bridges DENDRIMERS: second-generation third-generation
Steady-state rate: kSS Kalyanaraman and Evans, 2001
Photoinduced Electron Transfer through a dendrimer to acceptors diffusing in solution Aida et al, JACS 118 (1996) GOAL: to measure kET for electron transfer through the dendrimer framework
Simulations of solvent phase Photo-induced Electron Transfer to diffusing acceptors: Mallick and Evans, 2002 • Classical MD simulation of diffusing viologens • ET transfer rate to acceptors • Electron dynamics through the dendrimer following photoexcitation • (taking into account solvent dynamics)
Electron transfer rate from the dendrimer periphery to the diffusing viologens: Depends on time: Use Marcus expression with water as the solvent: ET to viologens is irreversible: treat the sites as absorbing boundary conditions
Classical Molecular Dynamics Simulations: NVE dynamics : dendrimer with viologen acceptors in water
Rate of transfer to viologen is • a dynamic variable that evolves along a simulation trajectory: L(t)
The second generation dendrimer: For the Aida experiments: rate is dominated by the intermolecular ET
The fourth generation dendrimer: Experimental studies: Observed kET = 2.6 × 109 s-1
Conclusions: • Electron transfer in dendrimers: • photo-induced • steady-state • Electron transfer rate depends on: • branching structure • enhanced over linear “wires” • solvent dynamics time-scale and coupling • strength • intermolecular ET rate to diffusing acceptors
Dendrimer RDF Malone, Evans 2000. r