Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Raymond R. Bard"'
Autor:
Valerie A. Walters, Julio C. de Paula, Ronda S. Bard, Raymond R. Bard, Gisela A. González-Montiel, Cesar Cornejo Ochoa, Triona Matheson, Justin Olson, Anthony Nguyen, David Ile, Anna K. Hicks, Elizabeth Gushtyuk, Matthew Foronda, Esther Chávez Álvarez, Miguel Ángel Cau Ontiveros
Publikováno v:
Journal of Archaeological Science: Reports. 43:103442
Publikováno v:
Journal of Chemical Crystallography. 46:429-434
Reaction of phloroglucinol with s-trinitrobenzene and triethylamine results in formation of the deep red bis-triethylammonium salt of 3,5,12-trinitrotricyclo[5.3.1.12,6]dodecan-8,10,11-trione-3,8-(NO2,O) dianion, [(C6H15NH)+]2 (C12H7N9)2−. Crystals
Publikováno v:
Journal of Chemical Education. 85:847
We present a safe and efficient technique to generate HCl/DCl gas for use in the classic physical chemistry experiment that introduces students to ro-vibrational spectroscopy. The reaction involves thionyl chloride and a mixture of water and deuteriu
Autor:
Raymond R. Bard, Michael J. Strauss
Publikováno v:
Journal of the American Chemical Society. 97:3789-3798
Publikováno v:
The Journal of Organic Chemistry. 43:2041-2044
Publikováno v:
The Journal of Organic Chemistry. 44:4918-4924
Autor:
Michael J. Strauss, Raymond R. Bard
Publikováno v:
The Journal of Organic Chemistry. 41:2421-2428
Autor:
Robert A. Ransdell, Paul Van Eikeren, Velu Senthilathipan, Valerie C. Anderson, Suzanne E. Clarke, John H. Golbeck, Douglas Alan Lorenz, James A. Yates, Dwayne Thomas Friesen, Donald R. Baer, Walter C. Babcock, Carl C. Wamser, John J. Sandberg, Gregory C. Stangle, Raymond R. Bard, Harold K. Lonsdale, George W. Rayfield
Publikováno v:
Journal of the American Chemical Society. 111:8485-8491
Thin polymeric porphyrin films have been prepared by interfacial polymerization of a pair of reactive comonomers, one or both of which are derivatized tetraphenylporphyrins. Combinations that have successfully yielded polymeric films include the foll
Autor:
Raymond R. Bard, Michael J. Strauss
Publikováno v:
The Journal of Organic Chemistry. 42:435-438
Publikováno v:
Journal of the American Chemical Society. 102:2852-2854
Arylhalogenide wie z.B. (I) reagieren mit dem Enolat (II) oder mit K in NH3 bei -33°C unter Bildung der Ketone (III) und der Alkohole (IV), deren Verhaltnis allein von der Abgangsgruppe bestimmt wird.