Effect of dicationic gemini surfactants 16-s-16 (s=4, 5, 6) on the ninhydrin-dipeptide (glycyl-tyrosine) reaction

被引:20
作者
Akram, Mohd [1 ]
Kumar, Dileep [1 ]
Kabir-Ud-Din [1 ]
机构
[1] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
关键词
AMINO-ACIDS; MICELLES; DECARBOXYLATION; CATALYSIS; PEPTIDES; PROTEINS;
D O I
10.1002/kin.20731
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
The effect of dicationic gemini surfactants H33C16(CH3)2N+-(CH2)s-N+(CH3)2 C16H33, 2Br- (s= 4, 5, 6) on the reaction of a dipeptide glycyltyrosine (GlyTyr) with ninhydrin has been studied spectrophotometrically at 70 degrees C and pH 5.0. The reaction follows first- and fractional-order kinetics, respectively, in [GlyTyr] and [ninhydrin]. The gemini surfactant micellar media are comparatively more effective than their single chainsingle head counterpart cetyltrimethylammonium bromide (CTAB) micelles. Whereas typical rate constant (k?) increase and leveling-off regions, just like CTAB, are observed with geminis, the latter produces a third region of increasing k? at higher concentrations. This subsequent increase is ascribed to the change in the micellar morphology of the geminis. The pseudophase model of micelles was used to quantitatively analyze the k? - [gemini] data, wherein the micellar-binding constants KS for [GlyTyr] and KN for ninhydrin were evaluated. (C) 2012 Wiley Periodicals, Inc. Int J Chem Kinet 44: 800809, 2012
引用
收藏
页码:800 / 809
页数:10
相关论文
共 32 条
[1]   Catalytic effect of CTAB on the interaction of dipeptide glycyl-tyrosine (Gly-Tyr) with ninhydrin [J].
Akram, Mohd ;
Kumar, Dileep ;
Kabir-ud-Din .
JOURNAL OF SAUDI CHEMICAL SOCIETY, 2014, 18 (05) :520-527
[2]  
Almog J, 1991, ADV FINGER PRINT TEC
[3]   Decarboxylation and dephosphorylation in new gemini surfactants. Changes in aggregate structures [J].
Brinchi, L ;
Germani, R ;
Goracci, L ;
Savelli, G ;
Bunton, CA .
LANGMUIR, 2002, 18 (21) :7821-7825
[4]  
Britton HTS., 1942, HYDROGEN IONS, V1
[5]   MICELLAR CATALYSIS OF ORGANIC-REACTIONS .34. NUCLEOPHILIC AROMATIC-SUBSTITUTION REACTIONS IN MICELLES WITH BULKY HEAD GROUPS [J].
BROXTON, TJ ;
CHRISTIE, JR ;
THEODORIDIS, D .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1993, 6 (09) :535-538
[6]   REACTION-KINETICS IN AQUEOUS SURFACTANT SOLUTIONS [J].
BUNTON, CA .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1979, 20 (01) :1-56
[7]   SPECIFIC MICELLAR RATE EFFECTS ON UNIMOLECULAR DECARBOXYLATION AND CYCLIZATION [J].
CERICHELLI, G ;
MANCINI, G ;
LUCHETTI, L ;
SAVELLI, G ;
BUNTON, CA .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1991, 4 (02) :71-76
[8]   SURFACTANT EFFECTS UPON CYCLIZATION OF O-(OMEGA-HALOALKOXY)PHENOXIDE IONS - THE ROLE OF PREMICELLAR ASSEMBLIES [J].
CERICHELLI, G ;
MANCINI, G ;
LUCHETTI, L ;
SAVELLI, G ;
BUNTON, CA .
LANGMUIR, 1994, 10 (11) :3982-3987
[9]   SECONDARY VALENCE FORCE CATALYSIS .8. CATALYSIS OF METHYL ORTHOBENZOATE BY ANIONIC SURFACTANTS [J].
DUNLAP, RB ;
CORDES, EH .
JOURNAL OF PHYSICAL CHEMISTRY, 1969, 73 (02) :361-&
[10]  
Fendler J.H., 1975, CATALYSIS MICELLAR M