DISTINCTION BETWEEN DIFFERENT COMPETING KINETIC-MODELS OF IRREVERSIBLE INTRAMOLECULAR 2-STATE EXCITED-STATE PROCESSES WITH ADDED QUENCHER - GLOBAL COMPARTMENTAL ANALYSIS OF THE FLUORESCENCE DECAY SURFACE

被引:18
|
作者
VANDOMMELEN, L
BOENS, N
DESCHRYVER, FC
AMELOOT, M
机构
[1] KATHOLIEKE UNIV LEUVEN,DEPT CHEM,B-3001 HEVERLEE,BELGIUM
[2] LIMBURGS UNIV CENTRUM,B-3590 DIEPENBEEK,BELGIUM
来源
JOURNAL OF PHYSICAL CHEMISTRY | 1995年 / 99卷 / 22期
关键词
D O I
10.1021/j100022a005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this report we investigate how, even in the absence of any a priori information, one can distinguish between competing irreversible intramolecular two-state excited-state processes. Only two different kinetic models are possible for irreversible intramolecular two-state excited-state processes: (i) one with a unidirectional excited-state process and (ii) one without an excited-state process. The distinction between these models is based on the collection of a fluorescence decay surface with at least three quencher concentrations and the use of standard global biexponential and global compartmental analyses. Standard global biexponential analysis provides estimates for the preexponential factors and decay times which, together with the steady-state fluorescence spectrum, allow the construction of decay-associated emission spectra. Two series of global compartmental analyses have to be performed whereby (i) k(01) is kept constant at various preset values while k(12) is held fixed at zero and whereby (ii) k(02) is scanned while k(21) is held constant at zero. k(0i) denotes the rate constant of deactivation of excited species i*, k(12) represents the rate constant of transformation of excited species 2* into 1*, and k(21) describes the opposite process. If negative preexponentials-indicative of a unidirectional excited-state process-are obtained in the global biexponential analysis, the statistical goodness-of-fit criteria of the repetitive global compartmental analyses allows one to determine the direction of the unidirectional excited-state process. When only positive preexponentials are obtained in the global biexponential analysis, the decay-associated emission spectra should be compared to the species-associated emission spectra. If both sets of spectra coincide, no excited-state process occurs. Otherwise, two solutions in which one rate constant of interconversion is zero are mathematically possible. It is impossible to distinguish between these two nontrivial alternative solutions.
引用
收藏
页码:8959 / 8971
页数:13
相关论文
共 16 条
  • [1] Distinction between different competing kinetic models of irreversible intramolecular two-state excited-state processes with added quencher. Global compartmental analysis of the fluorescence decay surface
    Van, Dommelen, L.
    Boens, N.
    De Schryver, F.C.
    Ameloot, M.
    Journal of Physical Chemistry, 1995, 99 (22):
  • [2] KINETICS AND IDENTIFIABILITY OF INTRAMOLECULAR 2-STATE EXCITED-STATE PROCESSES WITH ADDED QUENCHER - GLOBAL COMPARTMENTAL ANALYSIS OF THE FLUORESCENCE DECAY SURFACE
    BOENS, N
    AMELOOT, M
    HERMANS, B
    DESCHRYVER, FC
    ANDRIESSEN, R
    JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (04): : 799 - 808
  • [3] KINETICS AND IDENTIFIABILITY OF INTRAMOLECULAR 2-STATE EXCITED-STATE PROCESSES - GLOBAL COMPARTMENTAL ANALYSIS OF THE FLUORESCENCE DECAY SURFACE
    BOENS, N
    ANDRIESSEN, R
    AMELOOT, M
    VANDOMMELEN, L
    DESCHRYVER, FC
    JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (15): : 6331 - 6342
  • [4] SPECIES-ASSOCIATED SPECTRA AND UPPER AND LOWER BOUNDS ON THE RATE CONSTANTS OF REVERSIBLE INTRAMOLECULAR 2-STATE EXCITED-STATE PROCESSS WITH ADDED QUENCHER - GLOBAL COMPARTMENTAL ANALYSIS OF THE FLUORESCENCE DECAY SURFACE
    VANDOMMELEN, L
    BOENS, N
    AMELOOT, M
    DESCHRYVER, FC
    KOWALCZYK, A
    JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (45): : 11738 - 11753
  • [5] Experimental design in global compartmental analysis of reversible intramolecular two-state excited-state processes with added quencher
    Dutt, GB
    Boens, N
    Kowalczyk, A
    DeSchryver, FC
    Ameloot, M
    JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (11): : 1993 - 2002
  • [6] Fluorescence anisotropy decay for intramolecular two-state excited-state processes with added quencher in the presence of rotational diffusion: An identifiability analysis
    Szubiakowski, Jacek P.
    Dale, Robert E.
    Boens, Noel
    Ameloot, Marcel
    CHEMICAL PHYSICS LETTERS, 2007, 438 (1-3) : 113 - 118
  • [7] COMPARTMENTAL ANALYSIS OF FLUORESCENCE DECAY SURFACES OF EXCITED-STATE PROCESSES
    AMELOOT, M
    BOENS, N
    ANDRIESSEN, R
    VANDENBERGH, V
    DESCHRYVER, FC
    METHODS IN ENZYMOLOGY, 1992, 210 : 314 - 340
  • [8] EXPERIMENTAL-DESIGN IN THE GLOBAL COMPARTMENTAL ANALYSIS OF INTERMOLECULAR 2-STATE EXCITED-STATE PROCESSES
    VANDENBERGH, V
    KOWALCZYK, A
    BOENS, N
    DESCHRYVER, FC
    JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (38): : 9503 - 9508
  • [9] COMPARISON OF SIMULTANEOUS BIEXPONENTIAL AND COMPARTMENTAL ANALYSES OF FLUORESCENCE DECAY SURFACES OF INTERMOLECULAR 2-STATE EXCITED-STATE PROCESSES
    MEUWIS, K
    DEPUYDT, G
    BOENS, N
    DESCHRYVER, FC
    CHEMICAL PHYSICS LETTERS, 1995, 246 (06) : 641 - 648
  • [10] Intramolecular excited-state processes of a halato-telechelic polymer, evaluated by global compartmental analysis of the fluorescence decay surface with the use of model compounds
    vanStam, J
    DeSchryver, FC
    Boens, N
    Hermans, B
    Jerome, R
    Trossaert, G
    Goethals, E
    Schacht, E
    MACROMOLECULES, 1997, 30 (19) : 5582 - 5590