Role of functional groups and surfactant charge in regulating chlorophyll aggregation in micellar solutions

被引:46
作者
Agostiano, A
Catucci, L
Colafemmina, G
Scheer, H
机构
[1] Univ Bari, Dipartimento Chim, I-70126 Bari, Italy
[2] Univ Munich, Inst Bot, D-80638 Munich, Germany
[3] CNR, Ctr Studi Chim Fis Interaz Luce Mat, D-80638 Munich, Germany
关键词
D O I
10.1021/jp011718j
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
A series of modified chlorophylls, namely, pyrochlorophyll a, Zn-pheophytin a, Zn-pheophorbide a, chlorophyllide a, [3-acetyll]-chlorophyll a, and bacteriochlorophyll a, have been investigated in micellar solutions. The study is aimed at establishing the role played by the different functional groups of the chlorophyll in the molecular organization of chlorophylls in a microheterogeneous environment. The surfactants (AOT, CTAB. and Triton X-100) have been chosen mainly on the basis of the different charges carried by their polar heads, to study the effect of a point charge on the spectral characteristics of the pigments. Besides optical techniques used to investigate the spectral properties of the pigments, the state of the micellar system was studied by resonance light scattering (RLS) and NMR (self-diffusion and relaxation time measurements). The results of the UV-vis measurements evidence the role played by the functional group, or the chlorophylls in the formation of the different species in solution. In view of the few cases reported in the literature on blue-shifted chlorophyll species, special attention has been devoted, to the behavior of the modified chlorophylls in CTAB where a species absorbing around 6421 nm is always formed. CID, RLS, and NMR data identify this species as a pigment-surfactant aggregate, in which the positive charge of the surfactant interacts with the C-13(2) ketoester group of a monomeric chlorophyll.
引用
收藏
页码:1446 / 1454
页数:9
相关论文
共 62 条
[1]   SOLUBILIZATION MECHANISM OF CYTOCHROME-C IN SODIUM BIS(2-ETHYLHEXYL) SULFOSUCCINATE WATER OIL MICROEMULSION [J].
ADACHI, M ;
HARADA, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (14) :3631-3640
[2]   CHLOROPHYLL-A AUTOAGGREGATION IN WATER-RICH REGION [J].
AGOSTIANO, A ;
DELLAMONICA, M ;
PALAZZO, G ;
TROTTA, M .
BIOPHYSICAL CHEMISTRY, 1993, 47 (02) :193-202
[3]   Chlorophyll a self-organization in microheterogeneous surfactant systems [J].
Agostiano, A ;
Catucci, L ;
Colafemmina, G ;
Monica, MD .
BIOPHYSICAL CHEMISTRY, 1996, 60 (1-2) :17-27
[4]   Relevance of the chlorophyll phytyl chain on lamellar phase formation and organisation [J].
Agostiano, A ;
Catucci, L ;
Colafemmina, G ;
Della Monica, M ;
Scheer, H .
BIOPHYSICAL CHEMISTRY, 2000, 84 (03) :189-194
[5]   DIPOLE-DIPOLE TRANSFER BETWEEN ACETONE SOLVATES OF CHLOROPHYLL-A AND CHLOROPHYLL-A DIHYDRATE DIMERS IN WATER ACETONE MIXTURES - A MODEL FOR P680 SENSITIZED EXCITATION [J].
AGOSTIANO, A ;
BUTCHER, KA ;
SHOWELL, MS ;
GOTCH, AJ ;
FONG, FK .
CHEMICAL PHYSICS LETTERS, 1987, 137 (01) :37-41
[6]  
AGOSTIANO A, 1994, TRENDS PHOTOCHEM PHO, V3, P371
[7]   TRIPLET-STATE DECAY KINETICS OF HYDRATED CHLOROPHYLL COMPLEXES [J].
ALFANO, AJ ;
SHOWELL, MS ;
FONG, FK .
JOURNAL OF CHEMICAL PHYSICS, 1985, 82 (02) :765-772
[8]   COVALENTLY BOUND DIMERIC DERIVATIVE OF PYROCHLOROPHYLLIDE A - POSSIBLE MODEL FOR REACTION CENTER CHLOROPHYLL [J].
BOXER, SG ;
CLOSS, GL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (17) :5406-5408
[9]   ONE-ELECTRON OXIDATION OF PHOTOSYNTHETIC PIGMENTS IN MICELLES - BACTERIOCHLOROPHYLL-A, CHLOROPHYLL-A, CHLOROPHYLL-B, AND PHEOPHYTIN-A [J].
CHAUVET, JP ;
VIOVY, R ;
SANTUS, R ;
LAND, EJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1981, 85 (23) :3449-3456
[10]   CRYSTAL AND MOLECULAR-STRUCTURE AND ABSOLUTE-CONFIGURATION OF ETHYL CHLOROPHYLLIDE ALPHA DIHYDRATE - MODEL FOR DIFFERENT SPECTRAL FORMS OF CHLOROPHYLL-ALPHA [J].
CHOW, HC ;
SERLIN, R ;
STROUSE, CE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (25) :7230-7237