Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sulfur-containing molecules

UV-Vis spectroscopy may also provide valuable information if small molecules are studied. However, the photochemical sensitivity of many sulfur-containing molecules may trigger changes in the composition of the sample during irradiation. For instance, this phenomenon has been observed in Raman spectroscopy using the blue or green hnes of an argon ion laser which sometimes decompose sensitive sulfur samples with formation of Sg [2, 3]. Reliable spectra are obtained with the red hnes of a krypton ion or a He-Ne laser as well as with the infrared photons of a Nd YAG laser. [Pg.33]

Interest in the adsorption of sulfur-containing molecules at metal surfaces been stimulated by a desire to elucidate the decomposition mechanisms of thiols during the catalytic removal of sulfur from feedstocks and the position of thiols as the favoured head groups for adsorbates used to construct self-assembled monolayers. We shall not survey the extensive self-assembled film literature but restrict our discussion to the simpler thiols. [Pg.195]

Discusses constant interligand distances and has a large amount of structural information on sulfur containing molecules. [Pg.133]

A vast series of palladacycles derived from simple nitrogen-, oxygen-, and sulfur-containing molecules provide a good library for investigation of catalytic properties. Although elevated temperatures above 100 °C are necessary to awaken the catalysis with such complexes, the easy... [Pg.351]

Corrosion reactions of a metal with gaseous species such as oxygen, chlorine, sulfur containing molecules or water vapor to produce a thin layer of product phase are typical of ambipolar diffusion reactions. For example, metal oxidation... [Pg.241]

Whereas the variously catenated modifications of elemental sulfur can be satisfactorily treated by the MM method (207), organic sulfides and other sulfur-containing molecules suffer from the same polarization problem as do oxygen-containing molecules. Thus,... [Pg.151]

An enormous amount of work has been done in this wide field and a number of excellent reviews on different aspects of sulfur electrochemistry has been published [1-7], so here we confine our attention to some principal reactions and interesting apphcations of both anodic and cathodic activation of sulfur-containing molecules. Compared to other chalco-genides, sulfur has frontier orbitals that have volume, symmetry, and energy more suitable for efficient interaction with adjacent carbon atoms. The ionization of molecular sulfur requires about 10 eV. Conjugation of the pz orbitals of sulfur with a 7T-system lowers the ionization potential by ca. 2 eV. For this reason, compounds of divalent sulfur undergo oxidation rather easily often giving rise to cation radicals or dications. The stability of this species is in line with the... [Pg.237]

Gluck, S. J. The Response of the Model 700A Hall Electrolytic Conductivity Detector to Sulfur Containing Molecules Symposium On Environmental Analytical Chemistry, Brigham Young University, Paper IF, 1980. [Pg.175]

Systematic binding studies of a variety of Pt compounds with sulfur-containing molecules, which would eventually lead to the development of new antitumor drugs with structural properties such that the ratio of Pt binding at DNA compared to that of RSR is increased. [Pg.208]

There are two types of electronic transition commonly responsible for photochemically induced reactions in organic molecules. The first of these is the n—>ir transition in which an electron in a nonbonding atomic orbital is excited to an antibonding ir orbital, the excited state being referred to as n, it. This occurs in nitrogen-, oxygen-, and sulfur-containing molecules, and the nature of the n, 77 state of the carbonyl function has been the subject of considerable study.5,6 Excitation to the n, tt state in aldehydes and ketones occurs at approximately 290 nm. [Pg.2]

EXTENSIONS AND COMMENTARY This entire venture into the study of TOMSO was an outgrowth of the extraordinary response that had been shown by one person to 5-TOM. There were two obvious approaches that might throw some light on the reason for this dramatic sensitivity. One would be to see if he was unusually capable of metabolizing sulfur-containing molecules, and the second would be to assume he was, and to try to guess just what product he had manufactured with his liver. [Pg.228]

Barbour and Petersen (1974) observed strong H-bonding basicity of asphaltenes with phenol, having enthalpy of interactions between 6 and 8 kcal/mole. Phenol-base interactions for ir aromatic bases are typically as low as 0.5 kcal/mole but can reach 9 kcal/mole for nitrogen- or sulfur-containing molecules (Barton et al., 1972 Osawa et al., 1967 Whetsel, 1968). [Pg.121]

Among the oenological yeasts added during alcoholic fermentation, some strains of S. cerevisiae can use organic compounds to produce hydrogen sulfide and sulfites or the intermediate product of methionine (Zambonelli, 1988). These strains can use other sulfur-containing molecules, such as several of the pesticides employed in viticulture. [Pg.54]

The structural differences between the various sulfur-containing molecules make it impractical to have a single rate expression applicable to all reactions in hydrodesulfurization. Each sulfur-containing molecule has its own hydrogenolysis kinetics that is usually complex because several successive equilibrium stages are involved and these are often controlled by internal diffusion limitations during refining. [Pg.147]

There is a variety of sulfur-containing molecules in a residuum or heavy crude oil that produce different products as a result of hydrodesulfurization reaction. Although the deficiencies of current analytical techniques dictate that the actual mechanism of desulfurization remain largely speculative, some attempt... [Pg.165]

An obvious deficiency in the present marker study is that practically none of the other sulfur-containing molecules, known to be positive contributors to cooked-beef flavor, are detectable by this extraction and FPD gas chromatographic method (2-11. 20). The fate of more of these other contributors to the blend of cooked-beef flavor should also be studied to gain a better perspective. However, this extraction method is simple to use and is recommended for its reproducibility and high recovery of useful markers. [Pg.458]


See other pages where Sulfur-containing molecules is mentioned: [Pg.313]    [Pg.38]    [Pg.252]    [Pg.420]    [Pg.169]    [Pg.179]    [Pg.179]    [Pg.195]    [Pg.237]    [Pg.278]    [Pg.41]    [Pg.68]    [Pg.264]    [Pg.23]    [Pg.183]    [Pg.117]    [Pg.151]    [Pg.194]    [Pg.114]    [Pg.124]    [Pg.132]    [Pg.210]    [Pg.189]    [Pg.190]    [Pg.172]    [Pg.92]    [Pg.150]    [Pg.265]    [Pg.190]    [Pg.172]    [Pg.92]    [Pg.210]    [Pg.283]    [Pg.299]   
See also in sourсe #XX -- [ Pg.151 ]




SEARCH



Container molecule

Desulfurization sulfur-containing molecules

Interaction with sulfur-containing molecules

Sulfur-containing

© 2024 chempedia.info