Biochemical Synthesis and Unusual Conformational Switching of a Molecular Complex of Polyaniline and DNA

1999 ◽  
Vol 600 ◽  
Author(s):  
Ramaswamy Nagarajan ◽  
Sukant K. Tripathy ◽  
Jayant Kumar ◽  
Lynne A. Samuelson ◽  
Ferdinando F. Bruno

AbstractPolyaniline (Pani) is one of the most interesting conducting polymers because of its promising electrical properties and unique redox tunability. Recently a new template assisted, enzymatic synthetic approach has been developed which yields a water-soluble and conducting complex of polyaniline and the template used. The mild reaction conditions in this approach allow for the utilization of delicate biological systems as template materials, such as DNA. Here we report the extension of this enzymatic approach to the synthesis of Pani on a DNA matrix. DNA serves as a suitable template for complexation and formation of conducting polyaniline. The redox behavior of Pani induces reversible conformational change in the secondary structure of DNA. Circular dichroism results suggest that the secondary structure of the DNA may be reversibly switched through manipulation of the redox state of the polyaniline.

2004 ◽  
Vol 818 ◽  
Author(s):  
Sarswati Koul ◽  
Arokia Nathan

AbstractThe synthesis of water soluble nanomagnetic conducting polyaniline with an average particle size of 8nm ±1nm is presented. The particle growth morphology during reaction kinetics was controlled by using polyelectrolyte mediated dual oxidant-dopant system. The synthesis was carried out in a single reactor and the entire synthetic approach follows the principles of green chemistry. Dual oxidant-dopant system offers a solvent less chemical route for the synthesis of nanomagnetic polyaniline with maximum yield production.


Author(s):  
Andreas A Grauer ◽  
Burkhard König

Cα-Tetrasubstituted α-amino acids are important building blocks for the synthesis of peptidemimetics with stabilized secondary structure, because of their ability to rigidify the peptide backbone. Recently our group reported a new class of cyclic Cα-tetrasubstituted tetrahydrofuran α-amino acids prepared from methionine and aromatic aldehydes. We now report the extension of this methodology to aliphatic aldehydes. Although such aldehydes are prone to give aldol products under the reaction conditions used, we were able to obtain the target cyclic amino acids in low to moderate yields and in some cases with good diastereoselectivity.


1949 ◽  
Vol 22 (1) ◽  
pp. 232-244
Author(s):  
D. G. Fisher ◽  
J. R. Scott ◽  
W. H. Willott

Abstract Tests have been made on unloaded ebonites prepared from ordinary commercial types of natural rubber, special (deproteinized) rubbers having reduced contents of protein and(or) other water-absorbent substances, and a whole-latex rubber containing relatively large percentages of these substances, to determine to what extent these substances influence the electrical properties of the ebonite and, hence, whether any technically useful improvement can be effected by using specially prepared rubbers. Permittivity and power factor at 106 cycles per second, but particularly power factor, are somewhat improved by using the special rubbers, so that the dielectric loss can be reduced by about 30 per cent. In addition, the increase in dielectric loss caused by exposure to high humidity or by a rise of temperature is in general lessened by the use of these rubbers. Similar, though smaller, improvements in the properties of the ebonite are obtained by washing ordinary commercial rubber (smoked sheet). Although a definite improvement in dielectric loss is obtained, it does not seem probable that purification of natural rubber would lead to ebonites with dielectric properties approaching those of polystyrene, for instance. It seems unlikely that even complete elimination of the water-absorbent impurities would reduce the dielectric loss by more than 50 per cent; the rubber-sulfur compound itself thus appears to be responsible for a fair proportion of the loss normally observed. The large percentages of water-soluble substances present in whole-latex rubber increase the permittivity and especially the power factor of the ebonite made from it. The dielectric properties of ebonite are related, though not closely, to its water-absorbing capacity and that of the raw rubber used, low absorption being in general accompanied by low dielectric loss and reduced sensitiveness to humidity variations. There is only a rough parallelism between the water absorptions of raw rubbers and the corresponding ebonites. Probable reasons for this are indicated. It is concluded that water absorption tests on raw rubber form a useful, though only approximate, guide to its value for making electrical ebonite; electrical tests on the ebonite must be the final criterion. Apart from very impure whole-latex rubber, no correlation can be traced between the inorganic content (ash) of ebonite and its electrical properties. The probable reason for this is indicated. There is evidence that the dielectric loss of ebonite may increase with the passage of time. In view of its obvious theoretical and practical importance, this phenomenon requires further study. No technically useful advantage as regards breakdown strength, volume resistivity, surface resistivity, or stability to light, by the use of the special rubbers, is evident in the present work. The plastic yield characteristics of ebonite are not appreciably altered by using special rubbers. Estimations of uncombined sulfur and also plastic yield tests show that one of the deproteinized rubbers vulcanizes more rapidly than the rest, which differ little among themselves.


Pharmaceutics ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 794
Author(s):  
Halyna Kuznietsova ◽  
Natalia Dziubenko ◽  
Tetiana Herheliuk ◽  
Yuriy Prylutskyy ◽  
Eric Tauscher ◽  
...  

Excessive production of reactive oxygen species is the main cause of hepatocellular carcinoma (HCC) initiation and progression. Water-soluble pristine C60 fullerene is a powerful and non-toxic antioxidant, therefore, its effect under rat HCC model and its possible mechanisms were aimed to be discovered. Studies on HepG2 cells (human HCC) demonstrated C60 fullerene ability to inhibit cell growth (IC50 = 108.2 μmol), to induce apoptosis, to downregulate glucose-6-phosphate dehydrogenase, to upregulate vimentin and p53 expression and to alter HepG2 redox state. If applied to animals experienced HCC in dose of 0.25 mg/kg per day starting at liver cirrhosis stage, C60 fullerene improved post-treatment survival similar to reference 5-fluorouracil (31 and 30 compared to 17 weeks) and inhibited metastasis unlike the latter. Furthermore, C60 fullerene substantially attenuated liver injury and fibrosis, decreased liver enzymes, and normalized bilirubin and redox markers (elevated by 1.7–7.7 times under HCC). Thus, C60 fullerene ability to inhibit HepG2 cell growth and HCC development and metastasis and to improve animal survival was concluded. C60 fullerene cytostatic action might be realized through apoptosis induction and glucose-6-phosphate dehydrogenase downregulation in addition to its antioxidant activity.


Molecules ◽  
2020 ◽  
Vol 25 (2) ◽  
pp. 421 ◽  
Author(s):  
Daouda Ndiaye ◽  
Sébastien Coufourier ◽  
Mbaye Diagne Mbaye ◽  
Sylvain Gaillard ◽  
Jean-Luc Renaud

The development of efficient and low-cost catalytic systems is important for the replacement of robust noble metal complexes. The synthesis and application of a stable, phosphine-free, water-soluble cyclopentadienone iron tricarbonyl complex in the reduction of polarized double bonds in pure water is reported. In the presence of cationic bifunctional iron complexes, a variety of alcohols and amines were prepared in good yields under mild reaction conditions.


Synthesis ◽  
2018 ◽  
Vol 50 (24) ◽  
pp. 4897-4904 ◽  
Author(s):  
Ekaterina Stepanova ◽  
Andrey Maslivets ◽  
Svetlana Kasatkina ◽  
Maksim Dmitriev

A facile synthetic approach towards two distinct pyrrole-based heterocyclic scaffolds has been developed by the interaction of 1H-pyrrole-2,3-diones fused at the [e]-side to a 1,4-benzoxazin-2-one or quinoxalin-2(1H)-one moiety with ketones. The described interaction proceeds either as an aldol reaction or as a Michael addition/intramolecular cyclization depending on the reaction conditions. The disclosed aldol reaction proceeds with good diastereoselectivity under catalyst-free conditions when the reaction is carried out in aromatic hydrocarbons. Products of the cascade Michael addition/intramolecular cyclization reaction are predominantly formed under catalyst-free and solvent-free conditions. The proposed strategy provides facile access to pharmaceutically interesting pyrrole-based polyheterocycles.


2009 ◽  
Vol 7 (4) ◽  
pp. 769-773
Author(s):  
Vinodini Shaktawat ◽  
Dinesh Patidar ◽  
Kananbala Sharma ◽  
Narendra Saxena ◽  
Thansewar. Sharma

AbstractPure Polyaniline (EB) and Polyaniline doped with different protonic acids (ESs) were chemically synthesized using ammonium peroxydisulphate (APS) as an oxidant. Junctions have been prepared by evaporating chalcogenide materials (ZnSe, CdSe) on conducting polyaniline (EB & ESs) pellets using a vacuum evaporation technique. I–V characteristics of junctions have been studied at room temperature using the Keithley electrometer 6517A. I–V measurements show the rectification effect. A junction of ES[PO43−] may be preferred over the other junctions due to its low ideality factor and maximum rectification ratio.


1998 ◽  
Vol 548 ◽  
Author(s):  
Greg Vovk ◽  
Xiaohua Chen ◽  
Charles A. Mims

ABSTRACTAn in-situ XPS and voltammetry investigation of the redox properties of LaCrj1-xNixO3(x = 0.4, 1) was carried out by incorporating the materials as one electrode in an electrochemical cell (LaCr1xNixO3|YSZ|Pd:PdO), which was directly mounted on a heated sample stage in an ultra high vacuum (UHV) chamber. Under a 0.7V cathodic bias, the perovskites reduce from formal oxidation state of Ni3+ to Ni2+. This reduction is accompanied by wholesale shifts of the Cr and O core level binding energies, in keeping with the delocalized electronic states in the material. The adsorption properties of the surfaces are affected by the redox state of the surfaces; increased CO2adsorption is observed on the reduced (and therefore more basic) surface.


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