M Takahashi, M. Hoshino- Japan Probe Co. K. Kimura - Kimura Ultrasonic Testing Lab. Japan.  [c.902]

V. Pillai, P. Kumar, M. J. Hou, P. Ayyub, and D. O. Shah, Adv. Colloid Interface Sci, 55, 241 (1995).  [c.534]

V. Pillai, P. Kumar, M. S. Multani, and D. O. Shah, Colloids Surfaces, A80, 69 (1993).  [c.534]

P. Kumar, V. Pillai, and D. O. Shah, Appl. Phys. Lett., 62, 765 (1993).  [c.534]

Kumar A and Meath W J 1992 Dipole oscillator strength properties and dispersion energies for acetylene and benzene Mol. Phys. 75 311  [c.211]

Meath W J and Kumar A 1990 Reliable isotropic and anisotropic dipole dispersion energies, evaluated using constrained dipole oscillator strength techniques, with application to interactions involving H2, N2 and the rare gases Int. J. Quantum Chem. Symp. 24 501  [c.212]

Kunwar A C, Turner G L and Oldfield E 1986 J. Magn. Reson. 69 124  [c.1498]

Wallace C H, Rao L, Kim S-H, Heath J R, Nicol M and Kaner R B 1998 Solid-state metathesis reactions under pressure a rapid route to crystalline gallium nitride Appl. Phys. Lett. 72 596  [c.1965]

Kummer S, Mais S and Basche T 1995 Measurement of optical dephasing of a single terrylene molecule with nanosecond time resolution J. Chem. Phys. 99 17 078-81  [c.2508]

A. Kumar, P. K. Chowdhury, K. V. S. R. Rao, and J. P. Mittal, Chem. Phys. Lett. 182, 165(1991) A. Kumar, P. D. Naik, R. D. Sainy, and J. P. Mittal, Chem. Phys. Left. 309, 191 (1999).  [c.396]

SMD is a novel approach to the study of the dynamics of binding/unbinding events in biomolecular systems and of their elastic properties. The simulations reveal the details of molecular interactions in the course of unbinding, thereby providing important information about binding mechanisms. The advantage of SMD over conventional molecular dynamics is the possibility of inducing relatively large conformational changes in molecules on nanosecond time scales. Other methods, such as umbrella sampling, free energy perturbation (McCammon and Harvey, 1987), and weighted histogram analysis (Kumar ct ah, 1992), aiming at the determination of the energy landscapes, typically involve small conformational changes and require extensive computations to achieve accuracy.  [c.59]

H. Kawamura-Kuribayashi, N. Koga and K. Morokuma, J. Am. Chem. Soc. 114 (1992) 8687.  [c.441]

This synthesis of the pyrrole ring system, due to Knorr, consists in the condensation of an a-aminoketone with a 1,3-diketone or the ester of a p-keto-acid, a-Aminoketones are unstable in the free state, readily undergoing self-condensation consequently they must be prepared, by the reduction of an a-nitroso (or oximino) ketone, in the presence of the 1,3-diketone or p-ketoester, to ensure rapid interaction.  [c.293]

To meet the needs of the advanced students, preparations have now been included to illustrate, for example, reduction by lithium aluminium hydride and by the Meerwein-Ponndorf-Verley method, oxidation by selenium dioxide and by periodate, the Michael, Hoesch, Leuckart and Doebner-Miller Reactions, the Knorr pyrrole and the Hantzsch collidine syntheses, various Free Radical reactions, the Pinacol-Pinacolone, Beckmann and Arbusov Rearrangements, and the Bart and the Meyer Reactions, together with many others.  [c.585]

We are grateful to our colleagues for many valuable discussions and suggestions in particular we would mention Dr. F. B. Kipping, Dr. P. Maitland, Dr. G. W. Kenner and Mr. J. Harley-Mason.  [c.589]

Knoevenagel reaction Knorr pyrrole synthesis. Kolbe>Schmitt reaction Leuckart reaction Mannich reaction  [c.1210]

Another important inspection parameter to be controlled ist the appropriate UV-light intensity which is a control-parameter directly given by standards. To enable a CCD-Kamera to operate in a consistently reproducable mode at the focus point, the UV-Light intensity has to be compensated for aging of the UV-lamps. Figure 3 shows the time behaviour of the UV-light intensity. Our systems measure the UV-light intensity to be always above the given limit which enables the computer system to do the appropriate image processing.  [c.630]

K. Kimura Measurement of directivity for angle beam probe by side drilled holes and the effects of couplant thickness. Journal of JSNDI, Vol. 24, February, p88-89, (1975)  [c.908]

S. Ozawa, M. Goto, K. Kimura, and Y. Ogino, J. Chem. Soc., Faraday Trans. I, 80, 1049 (1984) S. Ozawa, K. Kawahara, M. Yamabe, H. Unno, and Y. Ogino, ibid, 80, 1059 (1984).  [c.427]

Kumar A, Fairley G R G and Meath W J 1985 Dipole properties, dispersion energy coefficients and integrated oscillator strengths for SFg J. Chem. Phys. 83 70  [c.211]

Kumar A, Meath W J, Bundgen P and Thakkar A J 1996 Reliable anisotropic dipole properties and  [c.212]

Jacob J, Kumar A, Anisimov M A, Povodyrev A A. and Sengers J V 1998 Crossover from Ising to mean-field critical behavior in an aqueous electrolyte solution Phys. Rev. E 58 2188  [c.553]

Resibois P and de keener M 1977 Ciassicai Kinetic Theory of Fiuids (New York Wiley)  [c.690]

In the early 1980s, it was shown that noisy light offers a time resolution of the order of the noise correlation time, of the light (typically tens to several hundreds of femtoseconds)—many orders of magnitude faster than the temporal profile of tlie light (which is often several nanoseconds, but in principle can be CW) [100, 101 and 102], A critical review of many applications of noisy light (including CRS) is given by Kobayashi [103], A more recent review by Kummrow and Lau [104] contains an extensive listing of references.  [c.1209]

Champion P M, Rosea F, Chang W, Kumar A, Christian J and Demidov A 1998 Femtosecond coherence spectroscopy of heme proteins XVith int. Conf on Raman Spectroscopy ed A M Heyns (New York Wley) pp 73-6  [c.1227]

Schaertel S A, Albrecht A C, Lau A and Kummrow A 1994 Interferometric coherent Raman spectroscopy with incoherent light some applications Appi. Rhys. B 59 377-87  [c.1229]

Kummrow A and Lau A 1996 Dynamics in condensed molecular systems studied by incoherent light Appi. Rhys. B 63 209-23  [c.1229]

Jimenez R, Fleming G R, Kumar P V and Maroncelli M 1994 Femtosecond solvation dynamics of water Nature 369 471-3  [c.1994]

Taylor-Maranas J K, Debenedetti P G, Graessley W W and Kumar S K 1997 Compressibility effeots in neutron soattering by polymer blends Macromolecules 30 6943  [c.2385]

Kummer S, Basche T and Brauchle C 1994 Terrylene in p-terphenyl a novel single crystalline system for single molecule spectroscopy at low temperatures Chem. Phys. Lett. 229 309-16  [c.2506]

Basche T, Kummer S and Brauchle C 1995 Direct spectroscopic observation of quantum ]umps of a single molecule Nature 373 132-4  [c.2507]

Kulzer F, Kummer S, Matzke R, Brauchle C and Basche T 1997 Single-molecule optical switching of terrylene in p-terphenyl Nature 387 688-91  [c.2508]

Tamarat P, Lounis B, Bernard J, Orrit M, Kummer S, Kettner R, Mais S and Basche T 1995 Pump-probe experiments with a single molecule ac-Stark effect and nonlinear optical response Phys. Rev. Lett. 75 1514-17  [c.2508]

Kumar A, Biebuyok FI A and Whitesides G M 1994 Patterning self-assembled monolayers—applioations in materials soienoe Langmuir 10 1498-511  [c.2637]

Kumar A, Biebuyck H A, Abbott N L and Whitesides G M 1992 The use of seif-assembied monoiayers and a seiective etch to generate patterned goid features J. Am. Chem. Soc. 114 9188-9  [c.2638]

Singhvi R, Kumar A, Lopez G P, Stephanopouios G N, Wang D i C, Whitesides G M and ingber D E 1994 Engineering ceii-shape and function Science 264 696-8  [c.2638]

Kumar K P, Keizer K and Burggraaf A J 1994 Stabiiization of the porous texture of nanostructured titania by avoiding a phase transformation J. Mater. Sc/. Lett. 59  [c.2924]

The preparation of 2 4-dimethyl-3 5-dicarbethoxypyrrole (II) is an example of the Knorr synthesis of pyrrole derivatives, involving the reaction of an -aminoketone (or a derivative thereof) with a reactive methylene ketone (or a derivative thereof). The stages In the present synthesis from ethyl acetoacetate (I) may be represented as follows  [c.839]

See pages that mention the term Kynar : [c.811]    [c.908]    [c.1477]    [c.2238]    [c.2428]    [c.2506]    [c.2637]    [c.2637]    [c.747]    [c.63]   
Plastics materials (1999) -- [ c.376 ]

Chemistry of Organic Fluorine compounds II (1995) -- [ c.1102 ]