Energy transfer in macromolecular arrays

被引:0
作者
Andrews, DL [1 ]
Jenkins, RD [1 ]
机构
[1] Univ E Anglia, Sch Chem Sci & Pharm, Norwich NR4 7TJ, Norfolk, England
来源
LINEAR AND NONLINEAR OPTICS OF ORGANIC MATERIALS III | 2003年 / 5212卷
关键词
energy transfer; exciton; bi-exciton; Forster; light-harvesting; photosynthesis; dendrimers; macromolecules;
D O I
10.1117/12.502375
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Macromolecular systems comprised of many light-sensitive centres (the photosynthetic unit, dendrimers, and other highly symmetric multichromophore arrays) are important structures offering challenges to theoreticians and synthetic chemists alike. Here we outline novel photophysical interactions predicted and observed in such arrays. Using the tools of molecular quantum electrodynamics (QED) we present quantum amplitudes for a variety of higher-order resonance energy transfer (RET) schemes associated with well-known nonlinear optical effects such as two- and three-photon absorption. The initial analysis is extended to account for situations where the participant donor species are identical and exist in a highly symmetric environment, leading to the possible formation of excitons. It emerges from the QED theory that such excitons are closely associated with the higher-order RET processes. General results are interpreted by analyzing particular molecular architectures which offer interesting features such as rate enhancement or limitation and exciton pathway quenching. Applications in the areas of photosynthesis, molecular logic gates and low-intensity fluorescence energy transfer are predicted.
引用
收藏
页码:250 / 261
页数:12
相关论文
共 23 条
[1]   Investigations of electronic energy transfer dynamics in multiporphyrin arrays [J].
Brodard, P ;
Matzinger, S ;
Vauthey, E ;
Mongin, O ;
Papamicaël, C ;
Gossauer, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (30) :5858-5870
[2]   Towards proper parametrization in the exciton transfer and relaxation problem:: dimer [J].
Cápek, V ;
Barvík, I ;
Herman, P .
CHEMICAL PHYSICS, 2001, 270 (01) :141-156
[3]  
Craig D. P., 1998, MOL QUANTUM ELECTROD
[4]   Resonance energy transfer: The unified theory revisited [J].
Daniels, GJ ;
Jenkins, RD ;
Bradshaw, DS ;
Andrews, DL .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (04) :2264-2274
[5]   Towards proper parametrization in the exciton transfer and relaxation problem.: II.: Trimer [J].
Herman, P ;
Barvík, I .
CHEMICAL PHYSICS, 2001, 274 (2-3) :199-217
[6]   Twin-donor systems for resonance energy transfer [J].
Jenkins, RD ;
Andrews, DL .
CHEMICAL PHYSICS LETTERS, 1999, 301 (3-4) :235-240
[7]   Three-center systems for energy pooling: Quantum electrodynamical theory [J].
Jenkins, RD ;
Andrews, DL .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (52) :10834-10842
[8]   Multichromophore excitons and resonance energy transfer: Molecular quantum electrodynamics [J].
Jenkins, RD ;
Andrews, DL .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (08) :3470-3479
[9]   A new diagrammatic methodology for non-relativistic quantum electrodynamics [J].
Jenkins, RD ;
Andrews, DL ;
Romero, LCD .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2002, 35 (03) :445-468
[10]   Four-center energy transfer and interaction pairs: Molecular quantum electrodynamics [J].
Jenkins, RD ;
Andrews, DL .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (15) :6713-6724