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1.
Kraineva J Narayanan RA Kondrashkina E Thiyagarajan P Winter R 《Langmuir : the ACS journal of surfaces and colloids》2005,21(8):3559-3571
We investigated the effect of incorporation of a small aqueous peripheral membrane protein (cyt c) into the three-dimensional periodic nanochannel structures formed by the lipid monoolein (MO) on its rich phase behavior as a function of temperature, pressure, and protein concentration using synchrotron X-ray small-angle diffraction. By simultaneous use of the pressure-jump relaxation technique and time-resolved synchrotron X-ray diffraction, we also studied the kinetics of various lipid mesophase transformations of the system for understanding the mechanistic pathways of their formation influenced by the protein-lipid interactions. Cyt c incorporated into the bicontinuous cubic phase Ia3d of MO has a significant effect on the lipid structure and the pressure stability of the system already at low protein concentrations. Concentrations higher than 0.2 wt % of cyt c led to an increase in interfacial curvature due to interaction of the protein with the lipid headgroups. This promotes the formation of a new, probably partially micellar cubic phase of crystallographic space group P4(3)32. Upon pressurization, the P4(3)32 phase undergoes a phase transition to a cubic Pn3m phase with smaller partial specific volume. Increase in protein concentration increases the pressure stability of the P4(3)32 phase. The formation of this phase from the cubic phase Pn3m is a slow process taking many seconds and having a time lag in the beginning. It seems to occur as a two-state process without ordered intermediate states. At temperatures above 60 degrees C, the P4(3)32 phase is unable to accommodate the unfolded protein and transforms to a bicontinuous cubic Ia3d phase. Time-resolved small-angle X-ray scattering studies show that the L(alpha) --> Ia3d transition in pure MO dispersions under limited hydration conditions occurs within a time interval of 1 s at 35 degrees C preceded by a lag phase of 1.5 s. The Ia3d cubic phase initially forms with a much larger lattice constant due to hydration and experiences an initially lower curvature that relaxes within about 1 s. Interestingly, no other cubic phases are involved as intermediates in the transition, i.e., the gyroid cubic phase is able to form directly from the L(alpha) phase. The mechanism behind the L(alpha) --> Ia3d transition in pure MO dispersions has been discussed within the framework of recent stalk models for membrane fusion. In the presence of cyt c, the L(alpha) --> Ia3d transition is much slower. The rather long relaxation times of the order of seconds are probably due to a kinetic trapping of the system and limitation by the transport and redistribution of water and lipid in the evolving new lipid phases. We also studied the transition from the pure lamellar L(alpha) phase to the Ia3d-P4(3)32 two phase region and observed a rather complex transition behavior with transient lamellar and cubic intermediate states. 相似文献
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Designed transition metal complexes predominantly catalyze Michael addition reactions. Inorganic and organic base‐catalyzed Michael addition reactions have been reported. However, known base‐catalyzed reactions suffer from the requirement of solvents, additives, high pressure and also side‐reactions. Herein, we demonstrate a mild and environmentally friendly strategy of readily available KOtBu‐catalyzed Michael addition reactions. This simple inorganic base efficiently catalyzes the Michael addition of underexplored acrylonitriles, esters and amides with (oxa‐, aza‐, and thia‐) heteroatom nucleophiles. This catalytic process proceeds under solvent‐free conditions and at room temperature. Notably, this protocol offers an easy operational procedure, broad substrate scope with excellent selectivity, reaction scalability and excellent TON (>9900). Preliminary mechanistic studies revealed that the reaction follows an ionic mechanism. Formal synthesis of promazine is demonstrated using this catalytic protocol. 相似文献
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Krishnan Thiyagarajan Thangavelu Kesavamurthy Gattu Bharathkumar 《Applied magnetic resonance》2014,45(3):255-268
Magnetic resonance imaging (MRI) technique is widely used to capture the images of the liquid items inside the human body. The radio-frequency (RF) coil is one of the important modules present inside an MRI system, which plays a major role in image quality. In this work, a microstrip-based high-pass RF birdcage coil is proposed for 1.5 T MRI. The cylindrical-shaped birdcage coil consists of 12 microstrip radiating elements and tuning capacitors to achieve a resonance at 63.85 MHz. The coil is made up of 10 mm polytetrafluoroethylene substrate coated by a conducting transmission line of desired length and width. A finite difference time domain simulation is carried out to analyze the return loss (S11), magnetic field homogeneity and Specific Absorption Rate (SAR) parameters of the RF coil. The SAR values of the proposed microstrip-based 1.5 T birdcage coil was compared with 3 T RF birdcage coil. The simulation results indicate the proposed birdcage coil structure gives optimal values of S11, magnetic field homogeneity and SAR. 相似文献
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Justin T. Russell Yao Lin Alexander Bker Long Su Philippe Carl Heiko Zettl Jinbo He Kevin Sill Ravisubhash Tangirala Todd Emrick Kenneth Littrell Pappannan Thiyagarajan David Cookson Andreas Fery Qian Wang Thomas P. Russell 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2005,117(16):2472-2478
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Chieh‐Tsung Lo Soenke Seifert Pappannan Thiyagarajan Balaji Narasimhan 《Macromolecular rapid communications》2005,26(7):533-536
Summary: The effect of polydispersity on polymer blend phase behavior is studied by in situ small‐angle X‐ray scattering. In a polydisperse polyethylene (PE)/isotactic poly(propylene) (iPP) blend, the enthalpic portion of the interaction parameter is greater than that of a corresponding blend with lower polydispersity. This is attributed to the presence of long chains, which provide a higher interaction energy and packing constraint, reducing the system miscibility. As expected, the radius of gyration is higher in the system with higher polydispersity.
8.
Matt J. Kipper Soenke Seifert P. Thiyagarajan Balaji Narasimhan 《Journal of Polymer Science.Polymer Physics》2005,43(5):463-477
Synchrotron small‐angle X‐ray scattering (SAXS) was used to study the isothermal crystallization kinetics of a family of polyanhydride copolymers consisting of 1,6‐bis(p‐carboxyphenoxy)hexane and sebacic acid monomers. In situ SAXS experiments permitted the direct observation of the crystallization kinetics. The structural parameters (the long period, lamellar thickness, and degree of crystallinity) were obtained from Lorentz‐corrected intensity profiles, one‐dimensional correlation functions, and interface distribution functions to form a comprehensive picture of the crystal morphology. The combination of these three analyses provided information not only on the lamellar dimensions but also on the polydispersity (nonuniformity) of these dimensions. Where possible, the crystallization kinetics were interpreted with a modified version of the Avrami equation. The results can be used to perform the rational design of controlled‐drug‐release formulations because crystallinity affects drug‐release kinetics. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 463–477, 2005 相似文献
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Pol VG Calderon-Moreno JM Thiyagarajan P 《Langmuir : the ACS journal of surfaces and colloids》2008,24(23):13640-13645
A single-step solvent-, catalyst-, and template-free synthesis process to prepare photoluminescent pencils of ZnO either in micro- or in nanosize diameters from a single precursor is demonstrated. The thermolysis of Zn's acetate dihydrate (ZAD) precursor in a closed stainless steel reactor at 700 degrees C under autogenic pressure (6.5 MPa), yielded carbon sphere-decorated ZnO micropencils (ZnO-M's). The ZnO-M's have novel room-temperature photoluminescence (PL) with well-defined emission peaks at the green, yellow, orange, and red regions of the visible spectra while suppressing the blue region. On the contrary, the thermolysis of ZAD in a closed stainless steel reactor at 700 degrees C with released pressure yielded uniformly carbon-coated ZnO nanopencils (ZN's). The coated carbon in ZN's quenches the complete UV-vis PL; however, after annealing ZN's at 600 degrees C/2 h in air, the UV PL is dominant, and the visible PL is suppressed. The carbon coating (partly or completely) on the one-dimensional (1D) ZnO surfaces plays an important role to modify PL properties. The insight into the reaction mechanism was gained through in situ mass spectrometry measurements. The as-prepared ZnO-M's and ZN's have been systematically characterized to determine their morphology, structure, and composition. 相似文献
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Thilak Kumar Thiyagarajan B. Mallikarjuna Rao Pallavi Vukkum Jamal Abdul Nasser Abhishek Singh Girish R. Deshpande 《Chromatographia》2008,68(11-12):919-926
A simple reverse phase liquid chromatographic method was developed for the quantitative determination of desipramine hydrochloride and its related impurities in bulk drugs which is also stability-indicating. During the forced degradation at hydrolysis, oxidative, photolytic and thermal stressed conditions, the degradation results were only observed in the oxidative stress condition. The blend of the degradation product and potential impurities were used to optimize the method by an YMC Pack Pro C18 stationary phase. The LC method employs a linear gradient elution with the water–acetonitrile–trifluoroacetic acid as mobile phase. The flow rate was 1.0 mL min?1 and the detection wavelength 215 nm. The stressed samples were quantified against a qualified reference standard and the mass balance was found close to 99.0% (w/w) when the response of the degradant was considered to be equal to the analyte (i.e. desipramine). The developed RP-LC method was validated in agreement with ICH requirements. 相似文献