Resolving the contribution due to Forster-type intramolecular electronic energy transfer in closely coupled molecular dyads

被引:29
作者
Alamiry, Mohammed A. H. [1 ]
Hagon, Jerry P. [1 ]
Harriman, Anthony [1 ]
Bura, Thomas [2 ]
Ziessel, Raymond [2 ]
机构
[1] Newcastle Univ, Sch Chem, Mol Photon Lab, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Strasbourg, Ecole Chim Polymeres & Macromol, Lab Chim Organ & Spect Avancees, F-67087 Strasbourg 02, France
基金
英国工程与自然科学研究理事会;
关键词
EXTENDED DIPOLE MODEL; DIELECTRIC-CONSTANT; REFRACTIVE-INDEX; HIGH-PRESSURE; SOLVENT; SINGLET; DYNAMICS; DENSITY; DEPENDENCE; MIGRATION;
D O I
10.1039/c2sc00948j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work examines the electronic energy-transfer (EET) processes inherent to a molecular dyad in which aryl polycycles attached to a boron dipyrromethene (Bodipy) dye act as ancillary light harvesters for near-UV photons. The solvent, being methyltetrahydrofuran, is compressed under applied pressure to such an extent that, over the accessible pressure range, there is a 25% decrease in molar volume. This effect serves to increase the effective concentration of the solute and increases fluorescence from Bodipy when this chromophore is excited directly. Illumination into the aryl polycycles, namely pyrene and perylene derivatives, leads to rapid intramolecular EET to Bodipy but fluorescence from these units is partially restored under high pressure. The argument is made that applied pressure restricts torsional motions around the linkages and imposes a near orthogonal geometry for transition dipole moment vectors on the reactants. In turn, this pressure-induced conformational restriction switches off Forster-type EET within the system, leaving the electron-exchange contribution. For the target dyad, the Forster component is ca. 5% for pyrene and ca. 25% for perylene. Such contributions are not inconsistent with calculations made on the basis of Forster theory but modelling is rendered difficult by the absence of accurate information about the nature of the conformational motion. Two possibilities have been considered. In the first case, the appendages remain stiff but pressure reduces the extent of displacement from the lowest-energy position. The results can be accounted for in a quantitative sense on the basis of small deviations from the lowest-energy conformation; the actual amount of displacement needed to explain the pressure effect depends on the method used to compute the Forster rates and ranges from ca. 4 degrees for the ideal dipole approximation to only 0.5 degrees for the extended dipole method. Secondly, pressure is assumed to bend each appendage into a banana-like shape. Again, the full effect of applied pressure can be accounted for by way of minor curvature of the linkage.
引用
收藏
页码:1041 / 1048
页数:8
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共 85 条
  • [1] Mechanistic principles and applications of resonance energy transfer
    Andrews, David L.
    [J]. CANADIAN JOURNAL OF CHEMISTRY, 2008, 86 (09) : 855 - 870
  • [2] Fullerene C60-Perylene-3,4:9,10-bis(dicarboximide) light-harvesting dyads:: Spacer-length and bay-substituent effects on intramolecular singlet and triplet energy transfer
    Baffreau, Jerome
    Leroy-Lhez, Stephanie
    Van Anh, Nguyen
    Williams, Rene M.
    Hudhomme, Pietrick
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (16) : 4974 - 4992
  • [3] Solvent and pH dependent fluorescent properties of a dimethylaminostyryl borondipyrromethene dye in solution
    Baruah, Mukulesh
    Qin, Wenwu
    Flors, Cristina
    Hofkens, Johan
    Valle, Renaud A. L.
    Beljonne, David
    Van der Auweraer, Mark
    De Borggraeve, Wim M.
    Boens, Noel
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (18) : 5998 - 6009
  • [4] Excitonic coupling in polythiophenes: Comparison of different calculation methods
    Beenken, WJD
    Pullerits, T
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (05) : 2490 - 2495
  • [5] Temperature-induced switching of the mechanism for intramolecular energy transfer in a 2,2′:6′,2"-terpyridine-based Ru(II)-Os(II) trinuclear array
    Benniston, AC
    Harriman, A
    Li, PY
    Sams, CA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (08) : 2553 - 2564
  • [6] Dynamics of electronic energy transfer in linear chain polymers
    Bodunov, EN
    Berberan-Santos, MN
    Martinho, JMG
    [J]. CHEMICAL PHYSICS LETTERS, 2001, 340 (1-2) : 137 - 141
  • [7] Molecular dynamics of covalently-linked multi-porphyrin arrays
    BothnerBy, AA
    Dadok, J
    Johnson, TE
    Lindsey, JS
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (44) : 17551 - 17557
  • [8] EFFECT OF SOLVENT POLARIZABILITY ON THE ULTRA-VIOLET SPECTRAL SHIFTS OF AROMATIC COMPOUNDS
    BOVEY, FA
    YANARI, SS
    [J]. NATURE, 1960, 186 (4730) : 1042 - 1044
  • [9] ENERGY-TRANSFER AND ELECTRON-TRANSFER PROCESSES INVOLVING PALLADIUM PORPHYRINS BOUND TO DNA
    BRUN, AM
    HARRIMAN, A
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (23) : 10383 - 10393
  • [10] Site torsional motion and dispersive excitation hopping transfer in π-conjugated polymers
    Brunner, K
    Tortschanoff, A
    Warmuth, C
    Bässler, H
    Kauffmann, HF
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (16): : 3781 - 3790