Search results for "Hexyne"

showing 3 items of 3 documents

Synthesis, Structural Analysis, Fiber Formation and Preliminary Anticancer Characterization of the Organotin Polyether from Dibutyltin Dichloride and…

2012

The organotin polyether derived from reaction of dibutyltin dichloride and 2,5-dimethyl-3-hexyne-2,5-diol was rapidly synthesized employing classical interfacial polymerization in 65% yield and a chain length of 360 units. IR results are consistent with the polyether structure. Bands characteristic of the formation of the Sn-O are present and bands characteristic of the Sn-Cl are absent. F MALDI MS results in the low mass range gives ion fragment clusters to five units. Isotopic abundance matches for tin are consistent with its presence in these ion fragment clusters. In the high mass range ion fragment clusters to greater than 300 units are found. The products offer outstanding inhibition …

AMPICILLINMALDI MSORGANOMETALLIC POLYMERSanomalous fiber formationANTIVIRAL ACTIVITYSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiCONTAINING POLYMERSOrganotin polyetherCONDENSATIONtin-containing polymerF MALDI MSSettore CHIM/03 - Chimica Generale E InorganicaNORFLOXACININTERFACIAL TECHNIQUEanticancer drugdibutyltin dichlorideMATRIXPOLYESTERS25-dimethyl-3-hexyne-25-diol
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CCDC 962938: Experimental Crystal Structure Determination

2014

Related Article: Ilya S. Krytchankou, Dmitry V. Krupenya, Antti J. Karttunen, Sergey P. Tunik, Tapani A. Pakkanen, Pi-Tai Chou, Igor O. Koshevoy|2014|Dalton Trans.|43|3383|doi:10.1039/C3DT52658E

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(mu~3~-((Phenylphosphinediyl)diethane-21-diyl)bis(diphenylphosphine))-bis(mu~2~-eta^2^-4-ethynyl-26-dimethylheptan-4-ol)-(mu~2~-3-hydroxy-3-isobutyl-5-methylhexyne-11-diyl)-tri-gold-silver hexafluorophosphate methanol solvate hydrateExperimental 3D Coordinates
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Development of MR active contrast agents via Parahydrogen Induced Polarization

2009

Parahydrogen Induced Polarization provides dramatic MR signal enhancement that can be exploited for molecular imaging. This method allows amongst others for Magnetic Resonance Imaging of 13C and 15N, which is usually constrained by the low MR sensitivity of these nuclei. By combining hydrogenation of barbiturates with parahydrogen under special experimental conditions (PASADENA under pressure) with a polarization transfer sequence we demonstrate the transfer of the initial 1H polarization to 13C. The polarization transfer yields a signal increase for 13C of more than 1000. Hence, the role of certain target compounds such as anesthetics like the barbituric acid derivatives could be investiga…

chemistry.chemical_compoundNuclear magnetic resonanceBarbituric acidChemistryHexeneHexyneHyperpolarization (physics)Molecular imagingSpin isomers of hydrogenPolarization (waves)Induced polarization
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