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31.
Nazar Mohammed Gabra Bakheit Mustafa Yata Praveen Kumar C. Shobha Devi A. Srishailam P. Venkat Reddy Kotha Laxma Reddy S. Satyanarayana 《Journal of fluorescence》2014,24(1):169-181
A new ligand 3-(1H-imidazo[4,5-f][1,10]phenanthrolin-2yl)phenylboronic acid and its (IPPBA) three ruthenium(II) complexes [Ru(phen)2(IPPBA)](ClO4)2 (1), [Ru(bpy)2(IPPBA)](ClO4)2 (2) and [Ru(dmb)2(IPPBA)](ClO4)2 (3) have been synthesized and characterized by elemental analysis, UV/VIS, IR, 1H-NMR,13C-NMR and mass spectra. The binding behaviors of the three complexes to calf thymus DNA were investigated by absorption spectra, emission spectroscopy, viscosity measurements, thermal denaturation and photoactivated cleavage. The DNA-binding constants for complexes 1, 2 and 3 have been determined to be 7.9?×?105 M?1, 6.7?×?105 M?1 and 2.9?×?105 M?1. The results suggest that these complexes bound to double-stranded DNA in an intercalation mode. Upon irradiation at 365 nm, three ruthenium complexes were found to promote the cleavage of plasmid pBR322 DNA from super coiled form ? to nicked form ??. Further in the presence of Co2+, the emission of DNA–Ru(ΙΙ) complexes can be quenched. And when EDTA was added, the emission was recovered. The experimental results show that all three complexes exhibited the “on–off–on” properties of molecular “light switch”. The highest Cytotoxicity potential of the complex1 was observed on the Human alveolar adenocarcinoma (A549) cell line. Good agreement was generally found between the spectroscopic techniques and molecular docked model which provides further evidence of groove binding. 相似文献
32.
Satyanarayana Reddy P. Veeranagaiah V. Ratnam C. V. 《Proceedings Mathematical Sciences》1975,81(3):124-131
Synthesis of 1-benzyl-3-methyl (I), 1-beazyl-3-substituted benzyl (II) and 1-methyl-3-substituted benzyl (III)-2-aryl benzimidazolines is described. (I) acc obtained by the condensation of N1benzyl-N2methyl-o-phenylenediamine with various aldehydes in metharol. Compounds (II) are prepared from N1-benzyl-N2-arylidene-o-phenylenediamines in acetic acid, through a process of disproportionation involving an oxidation-reduction process. Likewise, (III) are obtained from N1-methyl-N2-arylidenc-o-phenylenediamines. The exact structure of N1-benzyl-N2-arylidene-o-phenylenediamines which can exist in the open chain form or in the ring form has been investigated using nmr spectroscopy. 相似文献
33.
K. Praveen Kumar S. Satyanarayana P. Lakshmi Reddy G. Narasimhulu Narender Ravirala B.V. Subba Reddy 《Tetrahedron letters》2012,53(14):1738-1741
Iodine is found to be a highly efficient catalyst for the three-component coupling (3CC) of aldehydes, β-naphthol, and 1,3-dimethylbarbituric acid under solvent-free conditions to afford the corresponding 8,10-dimethyl-12-aryl-12H-naphtho[1′,2′5,6]pyrano[2,3-d]pyrimidine-9,11-diones in good yields with high selectivity. The use of readily available iodine makes this method very simple, convenient, and cost-effective. 相似文献
34.
Somepalli Venkateswarlu Meka Satyanarayana Gandrothu Narasimha Murthy Vidavalur Siddaiah 《Tetrahedron letters》2012,53(21):2643-2646
Cyclisation of 2-(2-aminophenyl)quinazolin-4(3H)-ones on to N3 and on to N1 leading to 6-alkyl-(8H)-quinazolino[4,3-b]quinazolin-8-one and 6-alkyl-(13H)-quinazolino[3,4-a]quinazolin-13-one, respectively was described for the first time. The differences in the IR and carbon NMR data of these isomeric fused quinazolinoquinazolinones afford a useful method for distinguishing between the two series. 相似文献
35.
BAQOR is a computer readable database for equilibrium constants in presence of different percentages of water miscible cosolvents. The present version with user friendly software in dBase III+ contains 740 records and runs on any IBM compatible PC. The physico-chemical properties of binary and ternary water-cosolvent mixtures, the equilibrium constants of proton- and metal-ligand complexes are retrievable through pop-up menus. Specific searches by metal-, ligand-, solvent-, and stoichiometry-wise and their combinations is possible. Several display modes-monitor, file and hard copy-are available for the numerical fields as well as for literature citation. 相似文献
36.
The first enantiospecific synthesis of allopupukeanones has been accomplished starting from 6-methylcarvone. A biogenetically patterned rearrangement of a pupukeanane to allopupukeanane was employed as the key step. 相似文献
37.
J. Satyanarayana V. N. Reddy G. S. Murty A. Dash 《Journal of Radioanalytical and Nuclear Chemistry》1994,188(5):323-330
Zirconium molybdoarsenate (ZrMAs), an inorganic ion exchanger, has been synthesized and the suitable conditions to separate cesium-137 from fission products waste solution are suggested. 相似文献
38.
Kudavalli JS Boyd DR Sharma ND More O'Ferrall RA 《The Journal of organic chemistry》2011,76(22):9338-9343
Acid-catalyzed dehydrations of substituted naphthalene-cis-1,2-dihydrodiols occur with loss of the 1- or 2-OH group to form 2- and 1-naphthols, respectively. Effects of substituents MeO, Me, H, F, Br, I, and CN at 3-, 6-, and 7-positions of the naphthalene ring are consistent with rate-determining formation of β-hydroxynaphthalenium ion (carbocation) intermediates. For reaction of the 1-hydroxyl group the 3-substituents are correlated by the Yukawa-Tsuno relationship with ρ = -4.7 and r = 0.25 or by σ(p) constants with ρ = -4.25; for reaction of the 2-hydroxyl group the 3-substituents are correlated by σ(m) constants with ρ = -8.1. The correlations for the 1-hydroxyl imply a surprisingly weak resonance interaction of +M substituents (MeO, Me) with a carbocation reaction center but are consistent with the corresponding correlation for acid-catalyzed dehydration of 3-substituted benzene-cis-1,2-dihydrodiols for which ρ = -6.9 and r = 0.43. Substituents at the 6- and 7-positions of the naphthalene rings by contrast are correlated by σ(+) with ρ = -3.2 for reaction of the 1-hydroxyl group and ρ = -2.7 for reaction of the 2-hydroxyl group. The unimpaired resonance implied by these substituent effects appears to be inconsistent with a previous explanation of the weak resonance of the 3-substituents in terms of imbalance of charge development and/or nonplanarity of the benzenium ring in the transition state. An alternative possibility is that the adjacent hydroxyl group interferes sterically with conjugation of +M substituents. "Hyperaromaticity" of the arenium ion intermediates does not appear to be a factor influencing this behavior. 相似文献
39.
Lawlor DA Kudavalli JS MacCormac AC Coyne DA Boyd DR O'Ferrall RA 《Journal of the American Chemical Society》2011,133(49):19718-19728
Cis- and trans-1,2-dihydrodiol isomers of benzene undergo acid-catalyzed dehydration to form phenol. In principle the isomeric substrates react through a common β-hydroxybenzenium (cyclohexadienyl) carbocation. Notwithstanding, the isomers show a large difference in reactivity, k(cis)/k(trans) = 4500. This difference is reduced to k(cis)/k(trans) = 440 and 50 for the 1,2-dihydrodiols of naphthalene and 9,10-dihydrodiols of phenanthrene, respectively, and to 6.9 for the dihydrodiols of the nonaromatic 7,8-double bond of acenaphthylene. Because the difference in stabilities of cis- and trans-dihydrodiols should be no more than 2-3-fold, these results imply a high cis stereoselectivity for nucleophilic trapping of a β-hydroxyarenium cation by water in the reverse of the carbocation-forming reaction. This is confirmed by studies of the 10-hydroxy-9-phenanthrenium ion generated from aqueous solvolyses of the trans-9,10-bromohydrin derivative of phenanthrene and the monotrichloroacetate ester of the phenanthrene cis-9,10-dihydrodiol. The cis stereoselectivity of forward and reverse reactions is explained by the formation (in the "forward" reaction) of different conformations of carbocation from cis- and trans-dihydrodiol reactants with respectively β-C-H and β-C-OH bonds in pseudoaxial positions with respect to the charge center of the carbocation optimal for hyperconjugation. Formation of different conformations is constrained by departure of the (protonated) OH leaving group from a pseudoaxial position. The difference in stability of the carbocations is suggested to stem (a) from the greater hyperconjugative ability of a C-H than a C-OH bond and (b) from enhanced conjugation arising from the stabilizing influence of an aromatic ring in the no-bond resonance structures representing the hyperconjugation (C(6)H(6)OH(+) ? C(6)H(5)OH H(+)). This is consistent with an earlier suggestion by Mulliken and a demonstration by Schleyer that the benzenium ion is subject to hyperconjugative aromatic stabilization. It is proposed that, in analogy with the terms homoconjugation and homoaromaticity, arenium ions should be considered as "hyperaromatic". 相似文献
40.
Satyanarayana Reddy Jaggavarapu Anand Solomon Kamalakaran Jagadeesh Babu Nanubolu Venkata Prasad Jalli Sravan Kumar Gangisetty Gopikrishna Gaddamanugu 《Tetrahedron letters》2014
Efficient and facile synthesis of 7H-benzopyrano[3,2-c]coumarins has been achieved by mild base promoted reaction of 4-chloro-3-formylcoumarin with diversely functionalized resorcinols. All the products were obtained as pure precipitates from the reaction mixture and the structure of the product was confirmed by X-ray analysis. 相似文献