Single-crystal X-ray diffraction studies of photo-induced molecular species

被引:82
作者
Cole, JM [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
关键词
D O I
10.1039/b205339j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This tutorial review gathers together the recent developments in single-crystal X-ray diffraction that are starting to enable one to quantify directly the nature of light-induced electronic perturbations in chemical structures. Such structural information is key to understanding many photo-activated chemical processes and physical properties, and a description of the scientific impetus behind this incipient area of structural science, from academic and industrial perspectives, is given. Photoisomerism processes, solid-state photochemical reactions and spin-cross-over magnetic transitions, that have long-lived or irreversible light-induced states, are best understood by unravelling their three-dimensional structures measured in situ in their photo-converted state. A review of steady-state laser-induced single-crystal X-ray diffraction studies conducted, to date, and the experimental methodologies used in order to realise such structures, is presented. The structural characterisation of more transient photo-induced species (down to picosecond lifetimes) is paramount to a better understanding of the materials that undergo high-speed electronic switching, which make operative much of the electronics and optics industry, since there exists an inherent relationship between the excited-state structure and the physical properties exhibited. Prime examples include excited-state structures of molecular conductors and luminescent materials with potential applications as molecular wires, light-emitting diodes, non-linear optics, triboluminescence and electroluminescence. Previously, only indirect and qualitative interpretations of the nature of these excited-states could be formulated via spectroscopic techniques, but the developments in ms-ps time-resolved laser pump, X-ray probe single-crystal diffraction techniques, described herein, are overcoming this barrier, affording results that are entirely quantitative via a three-dimensional structural representation. In this regard, a review of structures of transient species studied to date is presented along with a discussion of the key experimental parameters that are required for a successful experiment, in terms of the X-ray, laser and sample characteristics. The importance of auxiliary spectroscopic work and complementary theoretical calculations is also briefly discussed. The paper concludes with a future outlook on new possible X-ray sources that will facilitate such work and extend it to structural studies on even more ephemeral species in the future.
引用
收藏
页码:501 / 513
页数:13
相关论文
共 51 条
  • [1] Feasibility and realization of single-pulse laue diffraction on macromolecular crystals at ESRF
    Bourgeois, D
    Ursby, T
    Wulff, M
    Pradervand, C
    Legrand, A
    Schildkamp, W
    Laboure, S
    Srajer, V
    Teng, TY
    Roth, M
    Moffat, K
    [J]. JOURNAL OF SYNCHROTRON RADIATION, 1996, 3 : 65 - 74
  • [2] BRINKMAN WF, 1997, BELL LABS TECH J, P57
  • [3] Diffraction studies of photoexcited crystals: Metastable nitrosyl-linkage isomers of sodium nitroprusside
    Carducci, MD
    Pressprich, MR
    Coppens, P
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (11) : 2669 - 2678
  • [4] Taking snapshots of photoexcited molecules in disordered media by using pulsed synchrotron X-rays
    Chen, LX
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (22) : 2886 - 2905
  • [5] MLCT state structure and dynamics of a copper(I) diimine complex characterized by pump-probe X-ray and laser spectroscopies and DFT calculations
    Chen, LX
    Shaw, GB
    Novozhilova, I
    Liu, T
    Jennings, G
    Attenkofer, K
    Meyer, GJ
    Coppens, P
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (23) : 7022 - 7034
  • [6] Rapid excited-state structural reorganization captured by pulsed X-rays
    Chen, LX
    Jennings, G
    Liu, T
    Gosztola, DJ
    Hessler, JP
    Scaltrito, DV
    Meyer, GJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (36) : 10861 - 10867
  • [7] CLEGG W, SCIBLP0280101 DIAM L
  • [8] Nanosecond time-resolved crystallography of photo-induced species: case study and instrument development for high-resolution excited-state single-crystal structure determination
    Cole, JM
    Raithby, PR
    Wulff, M
    Schotte, F
    Plech, A
    Teat, SJ
    Bushnell-Wye, G
    [J]. FARADAY DISCUSSIONS, 2003, 122 : 119 - 129
  • [9] Laser-induced ferroelectric structural order in an organic charge-transfer crystal
    Collet, E
    Lemée-Cailleau, MH
    Buron-Le Cointe, M
    Cailleau, H
    Wulff, M
    Luty, T
    Koshihara, SY
    Meyer, M
    Toupet, L
    Rabiller, P
    Techert, S
    [J]. SCIENCE, 2003, 300 (5619) : 612 - 615
  • [10] Crystal engineering, solid state spectroscopy and time-resolved diffraction
    Coppens, P
    Ma, BQ
    Gerlits, O
    Zhang, YG
    Kulshrestha, P
    [J]. CRYSTENGCOMM, 2002, 4 : 302 - 309