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Deuterium Content (deuterium + content)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

Study of mineral water resources from the Eastern Carpathians using stable isotopes,

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 16 2009
Dana A. Magdas
The Eastern Carpathians contain many mineral water springs that feed famous Romanian health resorts such as Borsec, Biborteni and Vatra Dornei. These waters have been used for their different therapeutic effects. In this work, mineral and spring waters from these Romanian regions were investigated by means of chemical and isotopic (,D and ,18O) analyses in order to understand the recharge mechanisms and also to determine their origins. Most of the investigated springs are of meteoric origin, having the average deuterium content of the local meteoric water. The higher 18O content with respect to the Meteoric Water Line (MWL) indicated an exchange reaction with crystalline igneous rocks at depth and with other rocks that the water encounters on its journey back to the surface. Copyright © 2009 John Wiley & Sons, Ltd. [source]

A method for quantitative determination of deuterium content in biological material

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 6 2005
Yihui He
A method was developed for quantitative determination of deuterium incorporated into live organisms or biological macromolecules. The deuterated biological material was mixed with a bovine serum albumin (BSA) supporter to make a homogeneous sample for which the ,D value (vs. VSMOW) was analyzed using a dual-inlet gas isotope mass spectrometer. The method is described in detail, and the equation for calculation of deuterium content is presented, i.e., C,=,1/500,×,k,×,RVSMOW,×,C,×,106 ppm. Deuterated hepatitis A virus (HAV) RNA and BSA were systematically investigated. The results demonstrate that the method is capable of direct measurement of deuterium content, and is highly repeatable and reliable with a standard deviation of ±3,. It is stressed that the quantity of deuterated sample required is extremely small as a result of using BSA as supporter. The method may be applied in many fields, and has the strengths of simplicity, relative cheapness, and robustness. Copyright © 2005 John Wiley & Sons, Ltd. [source]

Synthetic Scope and Mechanistic Studies of Ru(OH)x/Al2O3 -Catalyzed Heterogeneous Hydrogen-Transfer Reactions

CHEMISTRY - A EUROPEAN JOURNAL, Issue 22 2005
Kazuya Yamaguchi Dr.
Abstract Three kinds of hydrogen-transfer reactions, namely racemization of chiral secondary alcohols, reduction of carbonyl compounds to alcohols using 2-propanol as a hydrogen donor, and isomerization of allylic alcohols to saturated ketones, are efficiently promoted by the easily prepared and inexpensive supported ruthenium catalyst Ru(OH)x/Al2O3. A wide variety of substrates, such as aromatic, aliphatic, and heterocyclic alcohols or carbonyl compounds, can be converted into the desired products, under anaerobic conditions, in moderate to excellent yields and without the need for additives such as bases. A larger scale, solvent-free reaction is also demonstrated: the isomerization of 1-octen-3-ol with a substrate/catalyst ratio of 20,000/1 shows a very high turnover frequency (TOF) of 18,400 h,1, with a turnover number (TON) that reaches 17,200. The catalysis for these reactions is intrinsically heterogeneous in nature, and the Ru(OH)x/Al2O3 recovered after the reactions can be reused without appreciable loss of catalytic performance. The reaction mechanism of the present Ru(OH)x/Al2O3 -catalyzed hydrogen-transfer reactions were examined with monodeuterated substrates. After the racemization of (S)-1-deuterio-1-phenylethanol in the presence of acetophenone was complete, the deuterium content at the ,-position of the corresponding racemic alcohol was 91,%, whereas no deuterium was incorporated into the ,-position during the racemization of (S)-1-phenylethanol-OD. These results show that direct carbon-to-carbon hydrogen transfer occurs via a metal monohydride for the racemization of chiral secondary alcohols and reduction of carbonyl compounds to alcohols. For the isomerization, the ,-deuterium of 3-deuterio-1-octen-3-ol was selectively relocated at the ,-position of the corresponding ketones (99,% D at the ,-position), suggesting the involvement of a 1,4-addition of ruthenium monohydride species to the ,,,-unsaturated ketone intermediate. The ruthenium monohydride species and the ,,,-unsaturated ketone would be formed through alcoholate formation/,-elimination. Kinetic studies and kinetic isotope effects show that the RuH bond cleavage (hydride transfer) is included in the rate-determining step. [source]