Polymeric Colorants: Statistical Copolymers of Indigo Building Blocks with Defined Structures

被引:7
|
作者
Voss, Gundula [1 ]
Drechsler, Markus [2 ]
Eller, Steffen [1 ]
Gradzielski, Michael [3 ]
Gunzelmann, Daniel [4 ]
Mondal, Svastik [5 ]
van Smaalen, Sander [5 ]
Voertler, Claus S. [6 ]
机构
[1] Univ Bayreuth, Dept Bioorgan Chem, D-95447 Bayreuth, Germany
[2] Univ Bayreuth, Dept Macromol Chem 2, D-95440 Bayreuth, Germany
[3] Tech Univ Berlin, Stranski Lab Phys & Theoret Chem, D-10623 Berlin, Germany
[4] Univ Bayreuth, Dept Inorgan Chem 1, D-95440 Bayreuth, Germany
[5] Univ Bayreuth, Dept Crystallog, D-95440 Bayreuth, Germany
[6] Univ Bayreuth, Dept Biochem, D-95440 Bayreuth, Germany
关键词
ABSORPTION-SPECTRA; COLLOIDS;
D O I
10.1002/hlca.200900123
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Statistical copolymers of indigo (1a) and N-acetylindigo (1b) building blocks with defined structures were studied. They belong to the class of polymeric colorants. The polymers consist of 5,5'-connected indigo units with keto structure and N-acetylindigo units with uncommon tautomeric indoxyl/indolone (=1H-indol-3-ol/3H-indol-3-one) structure (see 2a and 2b in Fig. 1). They formed amorphous salts of elongated monomer lengths as compared to monomeric indigo. The polymers were studied by various spectroscopic and physico-chemical methods in solid state and in solution. As shown by small-angle-neutron scattering (SANS) and transmission-electron microscopy (TEM), disk-like polymeric aggregates were present in concentrated solutions (DMSO and aq. NaOH soln.). Their thickness and radii were determined to be ca. 0.4 and ca. 80 nm, respectively. From the disk volumes and by a Guinier analysis, the molecular masses of the aggregates were calculated, which were in good agreement with each other. Defined structural changes of the polymer chains were observed during several-weeks storage in concentrated DMSO solutions. The original keto structure of the unsubstituted indigo building blocks reverted to the more flexible indoxyl/indolone structure. The new polymers were simultaneously stabilized by intermolecular H-bonds to give aggregates, preferentially dimers. Both aggregation and tautomerization were reversible upon dissolution. The polymers were synthesized by repeated oxidative Coupling of 1,1'-diacetyl-3,3'-dihydroxybis-indoles 5 (from 1,1'-diacetyl-3.3'-bis(acetyloxy)bis-indoles 6) followed by gradual hydrolysis of the primarily formed poly(N,N'-diacetylindigos) 7 (Scheme). N,N'-Diacetylbis-anthranilic acids 9 were isolated as by-products.
引用
收藏
页码:2675 / 2697
页数:23
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