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2.
V. Ramamoorthy A. Ramasubbu S. Muthusubramanian S. Sivasubramanian 《Journal of inclusion phenomena and macrocyclic chemistry》1999,33(1):69-80
The nitrone is found to be included in the -cyclodextrin cavity in two different stoichiometries viz., 1G : 1H and 1G : 2H – the existence of which is proved by physical methods. The 1G : 2H complex of the nitrone serves as a good potent dipolarophile in the 1,3-dipolar cycloaddition reactions with olefins resulting in rate acceleration and regioselection. 相似文献
3.
Kanthimathi Mookandi Unni Nair Balachandran Ramasami Thirumalachari Jeyakanthan Jeyaraman Velmurugan Devadasan 《Transition Metal Chemistry》2000,25(2):145-149
A new chromium(III) Schiff base complex, [Cr(3-methoxysalen)(H2O)2]ClO4, where salen=N,N-ethylenebis- (salicylideneimine), has been synthesized and characterized by spectroscopic techniques. Single crystal X-ray data reveals that the complex assumes a trans-diaquo structure with formulation [Cr(C18H22N2O6)]ClO4 but, unlike in Cr (salen)(H2O)2
+, the two trans-water molecules are equidistant from CrIII. The effect of the substituent on the phenyl ring in respect of redox reactivity has been investigated. The kinetics of the oxidation of [Cr(Schiff base)- (H2O)2]ClO4, where Schiff base=salen, (1) and 3-OMe-salen, (2) by PhOI has been studied. The bimolecular rate constant for the formation of the O=Crv Schiff base in case of (2) was four times faster than that of (1). The introduction of the OMe group substituent on the phenyl ring influences not only the structure and crystal packing, but also the reactivity of the complex and the electronic environment around the metal ion. 相似文献
4.
Venkatraman S Anand VG Pushpan SK Sankar J Chandrashekar TK 《Chemical communications (Cambridge, England)》2002,(5):462-463
Successful syntheses of two new aromatic core modified oxybenziporphyrins by a simple '3 + 1' methodology and the first aromatic core modified oxybenziporphyrin palladium complex are reported. 相似文献
5.
N. Ramasubbu R. Parthasarathy 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3-4):221-229
Abstract Using the Cambridge Crystallographic Data Base and computer retrieval methods, we have studied the preferred directions of approach of nucleophiles and electrophiles at divalent selenium centers. We find that electrophiles approach Se in a direction nearly normal to the selenide plane Y-Se-Z while nucleophiles approach Se nearly in the selenide plane and along the back side of Y-Se or Z-Se bonds. We also found evidence for the incipient formation of attractive electrophile-nucleophile pairing in Se…Se interactions. Other Se…Se contacts which did not fit the above pattern showed non-spherical effective shape for Se atoms. The preferred directions of approach of electrophiles and nucleophiles for Se and S are very similar and may be understood in terms of frontier orbitals. Such similarity in the shape and orbital environment of S and Se indicate to some extent how Se can play the role of S in some enzymes. 相似文献
6.
Two new fluorescent BODIPY dyes have been designed and synthesized. They dyes differ in their meso substituents, which have different electronic properties. Their selective reactivity towards an Ar‐SN2 reaction has been explored as a potential basis for colorimetric and fluorescent discrimination of primary, secondary and tertiary aliphatic amines. This dual‐mode, instantaneous recognition event is unprecedented. 相似文献
7.
Flavonoids are a group of plant phenolics that provide various health benefits through cell signalling pathways and antioxidant effects. In the present study, a new series of mixed ligand complexes of Co(II), Ni(II), Cu(II) and Zn(II) were synthesized by incorporating curcumin and quercetin flavonoid precursors. The structural features of the synthesized complexes were explored using elemental analysis, thermogravimetric analysis, UV–visible, infrared, NMR, mass and electron paramagnetic resonance spectral analyses and conductivity measurements. These data support an octahedral geometry of the synthesized complexes. In silico biological activity score for the ligand was predicted using PASS online software. ADMET properties were studied using VLS3D online software. Anti‐inflammatory and antioxidant activities were experimentally validated which prove that theoretical predictions are in agreement with the experimental results. Interestingly the synthesized complexes interact with calf thymus DNA through groove binding mode. Moreover, they have good potential to cleave pUC19 DNA. Minimum inhibitory concentration values of the synthesized complexes reveal that they have better antimicrobial efficacy than the ligands. 相似文献
8.
Sankar J Rath H Prabhuraja V Gokulnath S Chandrashekar TK Purohit CS Verma S 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(1):105-114
The synthesis and characterization of the first examples of core-modified corrole dimers linked through the meso positions are described. The dimers are obtained by a simple Ag(I)- or Fe(III)-catalyzed coupling reaction in near-quantitative yields. The corroles obtained are metalated with metal ions, such as Cu(II) and Ni(II). The electronic-absorption spectral studies reveal weak electronic interaction between the two subunits and the exciton coupling observed for the free-base corrole dimer (1717 cm(-1)) is lower than that for the corresponding protonated derivative (4081 cm(-1)). The solution-state structure derived from (1)H and two-dimensional NMR spectral studies reveals a noncoplanar arrangement of two corrole units. Geometry optimization at the B3LYP-631G level also confirms the noncoplanar arrangement of corroles with a dihedral angle of 64.8 degrees between two corrole planes. The electron paramagnetic resonance (EPR) and magnetic characterization studies on the paramagnetic copper-metalated dimer indicate that both copper ions behave as independent spins without any noticeable interaction. Results of fluorescence studies reveal a bathochromic shift of about 60 nm upon dimerization. The first hyperpolarizability (beta) measured by using the hyper Rayleigh scattering (HRS) method reveals doubling of the beta values on progressing from monomer to dimer, attributed to enhanced pi conjugation. The use of copper dimers in the photocleavage of DNA is also explored. It is shown that the bimetallic copper dimer selectively cleaves the nucleic acids without affecting the proteins, suggesting a possible application of the copper complex in the removal of nucleic acid contaminants from protein extracts through a simple photolytic pathway. 相似文献
9.
Venkatraman S Anand VG PrabhuRaja V Rath H Sankar J Chandrashekar TK Teng W Senge KR 《Chemical communications (Cambridge, England)》2002,(16):1660-1661
First successful syntheses and structural characterization of new core modified meso aryl azuliporphyrins by a simple [3 + 1] methodology are reported. 相似文献
10.
[reaction: see text] First examples of aromatic core-modified twisted heptapyrrolic systems with six meso links have been obtained via a general [3 + 4] acid-catalyzed condensation method. Despite the twisted conformation, these heptaphyrins exhibit aromaticity in solution, unlike most of the all-aza analogues. 相似文献