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1.
Synthesis and binding studies of new bis-calix[4]arenes containing aromatic and heteroaromatic units
A series of new bis-calix[4]arenes containing different aromatic and heteroaromatic moieties have been synthesized. The complexing behavior of these bis-calix[4]arenes have been studied towards different metal ions and it has been found that these bis-calix[4]arenes bind silver ions selectively over other metal ions. The complexation has been studied by liquid-liquid extraction and by NMR and IR spectroscopy. 相似文献
2.
S Chandrasekhar G Chandrashekar B Nagendra Babu K Vijeender K Venkatram Reddy 《Tetrahedron letters》2004,45(28):5497-5499
A facile synthesis of symmetrical and unsymmetrical ethers is achieved by reductive coupling of carbonyl compounds with alkoxysilanes. This reaction is performed using inert polymethylhydrosiloxane as the hydride source and B(C6F5)3 as the catalytic activator of the PMHS. 相似文献
3.
New PNA analogues derived from aminoethylpyrrolidin-5-one backbone show stabilization of aepone-PNA:DNA hybrids and destabilization of the corresponding RNA hybrids compared to unmodified PNA. 相似文献
4.
t-Butyl carbamates were obtained efficiently in high yields from the corresponding N-benzyl, N-trityl and N-diphenylmethyl precursors in a single-step reductive transformation employing polymethylhydrosiloxane and di-t-butyl dicarbonate under Pd(OH)2/C catalysis. 相似文献
5.
Summary New potential tetradentate ligands, N-benzoyl-N-thiobenzohydrazide (H2BTBH) and N-salicyl-N-thiobenzohydrazide (H2SBTH) have been prepared and characterized. Their complexes with CoII, NiII and ZnII have been prepared and characterized on the basis of elemental analyses, magnetic susceptibility measurements, and u.v.-vis., i.r. and 1H-n.m.r. spectral studies. The bonding and stereochemistries of the complexes are discussed. H2BTBH, H2SBTH and the complexes have been screened towards a number of bacteria. 相似文献
6.
7.
Manoj Kumar J. Nagendra babu Vandana Bhalla Navdeep Singh Athwal 《Supramolecular chemistry》2013,25(7):511-516
A new chromogenic receptor based on 1,2-phenylene derivative containing thiourea moieties is synthesized and examined for its anion binding ability by UV–Vis and 1H NMR studies. The results show that the receptor has selective colorimetric sensing of fluoride over all other anions like chloride, bromide, iodide, nitrate, hydrogen sulphate and acetate. 相似文献
8.
Synthetic peptides are in huge demand in expansion of potential peptide mimics, which may have improved or comparable function as natural one. With these concerns, phenyl bearing aromatic amino acids and peptides has extensively explored, because phenyl residue has high probability in forming stable secondary structure, owing to the presence of an extra stabilizing factor as π–π non-covalent interactions. Apart from phenyl bearing benzenoid aromatic amino acids, a few non-benzenoid aromatic derivatives such as tropolone and related compounds are also occurred in nature, but troponyl containing amino acids and peptides are very poorly understood. Tropolonyl derivatives also contain carbonyl functional group, which may play an important role to provide stable conformation in peptide. Herein we report the synthesis, and conformational analysis of rationally designed new unnatural δ-amino acid, troponyl aminoethylglycine (Tr-aeg), which contains troponyl residue as side chain in flexible aminoethylglycine (aeg) amino acid backbone. We also demonstrate the role of troponyl carbonyl of Tr-aeg residue in hydrogen bonding with adjacent amide NH of their hybrid di/tri-peptides with NMR methods and DFT calculations. In future, Tr-aeg amino acid would be a potential building block in development of promisable peptide mimics. 相似文献
9.
The aep-PNA is a chiral and cyclic PNA analogue, which has a stronger and base dependent binding affinity with complementary DNA. To understand the base dependent properties at monomer level, the structural studies of aep-PNA-(T/C/A) monomers have been carried out focussing on the conformational analysis of pyrrolidine ring pucker in aep-PNA by 1H NMR and the coupling constant data fitted into PSEUROT software. The results indicate that the type of pyrrolidine pucker depends on the electronic nature of substituent, implying the effect of pyrimidine or purine substituents in determining the ring pucker in monomers. This may consequently influence the aep-PNA oligomer conformation. Since pyrrolidine nucleic acids have emerged as an important class of PNA analogues, present results may have importance for their future development. 相似文献
10.
Gano JE Osborn DJ Kodali N Sekher P Liu M Luzik ED 《The Journal of organic chemistry》2003,68(9):3710-3713
Twist-twist pi-conjugated (TTPC) pi systems promise unique properties with their 90 degrees twist angles. Di-sec-alkyl substituted stilbenes, 5, were prepared by low-valent titanium coupling of phenyl ketones, 4. Long alkyl chains stopped the coupling reaction. Stilbenes 5 were shown to be approximately 90% TTPC. Inserting TTPC units into poly(p-phenylene) polymers created highly fluorescent, soluble, TTPC pi systems with weak electronic segmentation for organic light emitting diode (OLED) studies. 相似文献