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1.
A series of octahedral RuII/RuIII complexes of the type [Ru(Y)(CO)(BAX)(PPh3)2] and [RuCl2(BAX)(PPh3)2] (Y = H or Cl; BAX = benzaldehydeacetylhydrazone anion; X = H, Me, OMe, OH, Cl or NO2) have been prepared and characterised by spectral, magnetic and cyclic voltammetric studies. The RuII complexes are low spin diamagnetic (S = 0) whereas the RuIII complexes are low spin and paramagnetic (S = 1/2). These RuII and RuIII complexes absorb in the visible region respectively at ca. 16,000 and 28,000 cm–1 which bands are assigned to the MLCT. The correlation of the max values of the RuIII complexes with the + Hammett parameter, is linear, indicating the profound effect of substituents on the electron density of the central metal. I.r. spectral data reveals that the hydrazone is chelated to ruthenium through the hydrazinic nitrogen and the deprotonated enolic oxygen. The rhombic nature of the e.s.r. spectra of the RuIII complexes indicates an asymmetry in the electronic environment around the Ru atom. RuII complexes in CH2Cl2 show an irreversible RuII/III redox couple at ca. 0.9–0.5 V, while the RuIII complexes show two reversible redox couples in the –0.1–0.1 and 0.8–0.6 V range, indicating that the higher oxidation state of ruthenium is stabilised by hydrazones. 相似文献
2.
Vidya Rani Chandrasekhar Kesavan Mookkandi Palsamy Ravi Lokesh Daniel Thangadurai T. Indra Gandhi N. Rajesh Jegathalaprathaban Rajagopal Gurusamy 《应用有机金属化学》2019,33(3)
Three new metal complexes [Cu(L)2] (1), [Co(L)2] (2) and [Zn(L)2] (3) have been prepared by the reaction of hydrated salts of metal (II) acetate with new Schiff base ligand HL, [2‐((4‐(dimethylamino)phenylimino)methyl)‐4,6‐di‐t‐butylphenol] and characterized by different physico‐chemical analyses such as elemental analysis, single XRD, 1H NMR, FTIR and UV–Vis spectroscopic techniques. Their biomolecular docking, antimicrobial and cytotoxicity studies have also been demonstrated. The proposed structure of Schiff base ligand HL and complex 2 are confirmed by Single crystal X‐ray crystallography study. This analysis revealed that metal (II) complexes remain in distorted tetrahedral coordination environments. The electronic properties such as HOMO and LUMO energies are carried out by gaseous phase DFT/B3LYP calculations using Gaussian 09 program. Complex 1 showed a good binding propensity to the DNA and HSA, during the assessment of docking studies. Schiff base ligand HL and its metal (II) complexes, 1–3 screened for their in vitro antimicrobial activities using the disc diffusion method against selected microbes. Complex 1 shows higher antimicrobial activity than complexes 2, 3 and Schiff base ligand HL. According to the results obtained from the cytotoxic studies, Schiff base ligand HL and its metal (II) complexes 1–3 have better cytotoxicity against MCF‐7 cell lines with potency higher than the currently used chemotherapeutic agent cyclophosphamide. 相似文献
3.
Arumugam Vasudevan Gayathri Devi Gurusamy Rajkumar Kathiresan Sakthipandi Venkatachlam Rajendran Nallaiyan Rajendran Mani Rajkumar 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1434-1449
Abstract Phosphate-based bioactive glasses and their glass ceramics for 47P2O5– (30.5)CaO–(22.5 ? x)Na2O–xZrO2 for different ZrO2 contents (x = 0, 1.5, 3.0, 4.5, and 6.0 mol%) were prepared through melt quenching and controlled heat treatment procedures. The amorphous nature of glasses and the presence of crystalline phases in glass ceramics were studied by means of X-ray diffraction (XRD) studies. The density, molar volume, ultrasonic velocities, attenuation, elastic constants, and microhardness of glass and glass ceramics were used to study the structural changes. The formation of hydroxyapatite layer on the surface of glasses and glass ceramics after immersion in simulated body fluid (SBF) was explored through XRD, Fourier transform infrared (FTIR), and scanning electron microscopy (SEM) analyses. The results indicate that the added ZrO2 increases the crosslink density of glasses, resulting in network stability, and also induces the formation of an apatite layer on the surface of glasses. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
4.
5.
Surabhi Gupta Popuri Sureshbabu Adesh Kumar Singh Shahulhameed Sabiah Jeyakumar Kandasamy 《Tetrahedron letters》2017,58(10):909-913
A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies. 相似文献
6.
Indhumathi Kulandhaisamy Dinesh Babu Rajendran Malathi Kanagasabai Gunasekaran Gurusamy Balaji Moorthy Jithila V. George 《Waves in Random and Complex Media》2017,27(1):38-46
In this paper, an analog multiband phase shifter using slotline configuration is proposed. To implement the design, a pair of modified Split Ring Resonator (SRR) is employed. The periodic property of SRR provides multiband characteristics, whether the coupling slot gives the phase variations over the bands. The operation is well explained with an equivalent circuit model and its characteristics have been studied both in simulation and measurement. The prototype operates in 1.77–2.16, 3.5–3.97, 5.08–5.33, 6.43–6.93, and 8.01–8.59 GHz frequency bands which can be utilized for GSM, GPS, WLAN, C-band, and X-band applications, respectively. 相似文献
7.
Gurusamy Rajagopal Shanmugam Selvaraj Karuthamohamed Dhahagani 《Tetrahedron: Asymmetry》2010,21(18):2265-2270
Various ketones have undergone asymmetric trimethylsilylcyanation at room temperature with (CH3)3SiCN (TMSCN) in the presence of a chiral-supported Cu(salen) complex and Ph3PO as the catalyst. Aromatic, aliphatic, and heterocyclic ketones have been converted into the corresponding cyanohydrin trimethylsilyl ethers in 83?96% yields with 52?84% ee. Several factors concerning the reactivity and enantioselectivity have been discussed. A double activation where Cu(salen) plays the role of Lewis acid and Ph3PO acts as a Lewis base is reported. Poly(ethylene glycol) monomethyl ether (MeO-PEG) has been used as a soluble support while JandaJel (JJ) and Merrifield (MF) resins served as insoluble supports. Each polymer is linked to the salen catalyst through a glutarate spacer. The soluble catalysts were recovered by precipitation with a suitable solvent while the insoluble catalysts were simply filtered from the reaction mixture. The JandaJel-attached Cu(salen) catalyst could be used for five cycles with the retention of efficiency and the Merrifield-bound Cu(salen) catalyst was found to loose activity with each use. 相似文献
8.
Pradeepa Prabakaran Ramesh Prabhu Manimuthu Sowmya Gurusamy 《Journal of Solid State Electrochemistry》2017,21(5):1273-1285
Organic-inorganic hybrid membranes based on poly(ethylene oxide) (PEO) 6.25 wt%/poly(vinylidene fluoride hexa fluoro propylene) [P(VdF-HFP)] 18.75 wt% were prepared by using various concentration of nanosized barium titanate (BaTiO3) filler. Structural characterizations were made by X-ray diffraction and Fourier transform infrared spectroscopy, which indicate the inclusion of BaTiO3 in to the polymer matrix. Addition of filler creates an effective route of polymer-filler interface and promotes the ionic conductivity of the membranes. From the ionic conductivity results, 6 wt% of BaTiO3-incorporated composite polymer electrolyte (CPE) showed the highest ionic conductivity (6 × 10?3 Scm?1 at room temperature). It is found that the filler content above 6 wt% rendered the membranes less conducting. Morphological images reveal that the ceramic filler was embedded over the membrane. Thermogravimetric and differential thermal analysis (TG-DTA) of the CPE sample with 6 wt% of the BaTiO3 shows high thermal stability. Electrochemical performance of the composite polymer electrolyte was studied in LiFePO4/CPE/Li coin cell. Charge-discharge cycle has been performed for the film exhibiting higher conductivity. These properties of the nanocomposite electrolyte are suitable for Li-batteries. 相似文献
9.
Nagarajan S Taskent-Sezgin H Parul D Carrico I Raleigh DP Dyer RB 《Journal of the American Chemical Society》2011,133(50):20335-20340
The time scale for ordering of the polypeptide backbone relative to the side chains is a critical issue in protein folding. The interplay between ordering of the backbone and ordering of the side chains is particularly important for the formation of β-sheet structures, as the polypeptide chain searches for the native stabilizing cross-strand interactions. We have studied these issues in the N-terminal domain of protein L9 (NTL9), a model protein with mixed α/β structure. We have developed a general approach for introducing site-specific IR probes for the side chains (azide) and backbone ((13)C═(18)O) using recombinant protein expression. Temperature-jump time-resolved IR spectroscopy combined with site-specific labeling enables independent measurement of the respective backbone and side-chain dynamics with single residue resolution. We have found that side-chain ordering in a key region of the β-sheet structure occurs on a slower time scale than ordering of the backbone during the folding of NTL9, likely as a result of the transient formation of non-native side-chain interactions. 相似文献
10.
The addition of TMSCN to ketones catalyzed by dispersed NbF5 gave corresponding cyanohydrin trimethylsilylethers with excellent yield (>90%). Cyano transfer occurs within 30 min at room temperature in the presence of 1 mol% of NbF5 under solvent‐free conditions. These conditions are extremely mild, simple, and tolerate various functional groups. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献