Big Chemical Encyclopedia

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

Articles Figures Tables About

Dalton reaction

Thrombin, the two-chain derivative of the prothrombin molecule, has a molecular weight of approximately 37,000 daltons. Its proteolytic properties induce the conversion of fibrinogen to fibrin to produce the initial visible manifestation of coagulation, the soluble fibrin clot. In addition, thrombin influences the activity of Factors V, VIII, and XIII and plasmin. Thrombin affects platelet function by inducing viscous metamorphosis and the release reaction with subsequent aggregation. [Pg.173]

Factor XIII. Factor XIII circulates in the blood as a zymogen composed of two pairs of different polypeptide chains designated A and B. Inert Factor XIII has a molecular weight of 350,000 daltons and is converted to its active transglutaminase form in the presence of thrombin and calcium. Activated Factor XIII, Xllla, induces an irreversible amide exchange reaction between the y-glutamine and S-lysine side chains of adjacent fibrin... [Pg.174]

On the basis of Dalton s theory, the atom can be defined as the smallest particle of an element that can enter into a chemical reaction. [Pg.26]

Dalton s atomic theory explained three of the basic laws of chemistry The law of conservation of mass This states that there is no detectable change in mass in an ordinary chemical reaction. If atoms are con-... [Pg.28]

The MW of the TBDMS derivatives of PTH-AAs can be calculated using the following formula MW = R + 191 + n(114), where n is the number of TBDMS groups. Arginine loses NH3 during, or prior to, the derivatization reaction. Thus, the characteristic loss of 57 Daltons (C4H9) from the TBDMS derivative occurs at M - 74 (57 + 17). [Pg.54]

Guss, J. M. Mason, R. (1973) Reactions of [14]annulene and dehydro[14]annulene with organotricarbonylchromium complexes Crystal and molecular structures of hexacarbonyl-trans-6a,12a-dihydrooctalenedichromium(0), tricarbonyl-1,4-dihydrophenanthrenechromium(O), and tricarbonylphen-anthrenechromium(O), J. Chem. Soc. Dalton Trans., 1834— 1840. [Pg.245]

The change in a state function can be determined without knowing the details of a process, because that change is independent of path. Denver is 950 miles from San Francisco, no matter how the Daltons travel between the two cities. This means that state function values can be tabulated and looked up when needed. The distance from San Francisco to Denver can be found in an atlas of the United States. Energy is a state function, and changes in energy that accompany standard chemical reactions are tabulated in reference books such as the CRC Handbook of Chemistry and Physics. [Pg.371]

Gaseous solutions are easy to prepare and easy to describe. The atoms or molecules of a gas move about freely. When additional gases are added to a gaseous solvent, each component behaves independently of the others. Unless a chemical reaction occurs, the ideal gas equation and Dalton s law of partial pressures describe the behavior of gaseous solutions at and below atmospheric pressure (see Chapter 5). [Pg.829]

The viscosity of the 20 mg/mL PGA solution was too high to be filtered by the 2000 daltons cut-off membrane. In direct filtration or filtration experiments at the earliest stages of the enzymatic degradation, a gel appeared between the hollow fibers of the cartridge, which meant that we had to keep the reaction without filtration for 6 hours (until the viscosity of the system was adequate). [Pg.985]

The degradation of nicotine has been examined extensively in Arthrobacter nicotinovorans (oxydans) in which it is mediated by a plasmid (Brandsch et al. 1982 Schenk et al. 1998). In strain P34, the hrst metabolite was 6-hydroxynicotine, and experiments with 02 and H2 0 showed that the oxygen in the hydroxyl group was derived from H2O (Hochstein and Dalton 1965). Nicotine dehydrogenase has a molecular mass of 120,000 and contains FAD, Mo, Fe, and acid-labile sulfur (Freudenberg et al. 1988). Degradation involves a series of reactions ... [Pg.532]

Constable, E.C., Henney, R.P.G., Leese, T.A. and Tocher, D.A. (1990) Cyclometallation reactions of 6-phenyl-2,2 -bipyridine a potential C,N,N-donor analogue of 2,2 6, 2"-terpyridine. Crystal and molecular structure of dichlorobis (6-phenyl-2,2 -bipyridine)ruthenium(II). Journal of the Chemical Society, Dalton Transactions, (2), 443. [Pg.82]

Cyclometallation reactions of 6-(thienyl)-2,2 -bipyridine with d transition metal ions. Journal of the Chemical Society, Dalton Transactions, (14), 2251. [Pg.82]

Kitadai, K., Takahashi, M., Takeda, M., Bhargava, S.K., Priver, S.Fl. and Bennett, M.A. (2006) Synthesis, structures and reactions of cyclometalated gold complexes containing (2-diphenylarsino-n-methyl)phenyl (n = 5, 6). Dalton Transactions, (21), 2560—2571. [Pg.170]

Byers, P.K, Carr, N. and Stone, F.G.A. (1990) Chemistry of polynuclear metal complexes with bridging carbene or carbyne ligands. Part 106. Synthesis and reactions of the alkylidyne complexes [M ( CR)(CO)2 (C6F5)AuC(pz)3 j (M = W or Mo, R — alkyl or aryl, pz — pyrazol-l-yl) crystal structure of pjC PtAu(C6F5)( l3-CMe)(CO)2(PMe2Ph)2 (C6F5)AuC(pz)3 ]. Journal of the Chemical Society, Dalton Transactions, (12), 3701—3708. [Pg.173]

Uson, R., Laguna, A., Vdlacampa, M.D., Jones, P.G. and Sheldrick, G.M. (1984) Reactions of cis-diisocyanidebis (perfluorophenyl)gold(III) complexes with hydrazines. Crystal and molecular structure of bis(perfluorophenyl)[3-phenyl-l,4-bis(p-toluidino)-2,3-diazabut-l-en-l-yl-4-ylidene]gold. Journal of the Chemical Society, Dalton Transactions, (9), 2035-2038. [Pg.176]

Insulin, a small protein of molecular mass 6000 daltons, is composed of two chains designated A and B. There are no reduced cysteine residues in insulin, but it contains three essential disulfide bonds two that crosslink the A and B chains, and one internal to the A chain to stabilize the overall tertiary stmcture. These disulfide bonds are cleaved in the presence of excess AuX4, leaving A and B chains that have cysteine residues that have become oxidized to sulfonic adds [119]. With smaller amounts of AuX4, a single disulfide bond will be attacked to form sulfinic acid [119]. The reaction is second order for AuCU while AuBr4 reacts too quickly for accurate monitoring. [Pg.301]

Synthesis of 5,10,15,20-Tetrakis(4-(polyethyleneoxy)phenyl)) porphyrin. A slurry of polyethylene methylsulfonic ester (PEvoo-OMs) (20.0 g, 69% functionalized, Mn -780 Daltons) and anhydrous cesium carbonate (CS2CO3) (9.05 g, 27 mmol) in dry toluene (75 ttiL) was prepared and to this mixture a purple solution of 5,10,15,20-tetrakis(4-hydroxyphenyl)-21H,23H-porphine (2.9 g, 4.27 mmol) in 75 mL A. A-DMF was added. The reaction mixture was warmed to 95°C with stirring for 18 hours, then the temperature increased to 130°C for a further 5 hours before coohng. The purple-brown solid was collected by filtration, washed thoroughly with methanol and dried under vacuum to yield 21.0 g of the crude ligand, h NMR (toluene-dg, 80°C) 5 8.96 (s), 8.10 (d), 7.22 (d), 4.05 (t), 1.88 (quia), 1.58 (quin.), 1.31 (br. s), 0.88 (t). [Pg.322]

Synthesis of Polyethylene-tethered Phthalonitrile. Polyethylene monoalcohol ( 700 Daltons, 80% functionalized) in pellet form (6.0 g, 8.0 mmol) and anhydrous THF (62 mL) were added to a flask equipped with a magnetic stirring bar. This was allowed to stir for 2 hours before 4-nitrophthalonitrile (2.25 g, 13.0 mmol) was added to the mixture and the suspension heated to reflux. After the polymer had dissolved the CS2CO3 (4.22 g, 13.0 mmol) was added in three equal portions over 3 hours. After 24 hours the reaction was cooled to 60°C then poured into 500 mL of water with stirring. The precipitate was filtered and washed thoroughly with water until pH neutral. The product was then rinsed with A, V-DMF, THF and then dried under vacuum to yield 5.03 g of material. H NMR (toluene-dg, 100°C, 71% conversion) 5 6.86 (d), 6.59 (s), 6.41 (m), 3.41 (t), 3.37 (t), 1.31 (s), 0.88 (t). [Pg.323]

One of the more difficult to manage aspects of compound reactivity is the potential for idiosyncratic immunological reactions to covalent protein-compound complexes. Normally the immune system does not respond to xenobiotics of molecular weight less than 1000 Daltons. When, however, a drag is covalently linked to a... [Pg.225]

The Marshall group has optimized reaction (14) to obtain a poly-si lazane with Mw A000 Daltons which can be hand drawn to give 10-20 pm preceramic fibers. These fibers are then rendered Infusible by exposure to humid air and pyrolyzed to give fibers with the same ceramic yields, 55+%, as found by Verbeek et al. The ceramic products are mainly amorphous SiC and SijN with some Si02 (a consequence of the humidity treatments). [Pg.131]

Dalton argued that these laws are entirely reasonable if the elements are composed of atoms. For example, the reason that mass is neither gained nor lost in a chemical reaction is that the atoms merely change partners with each other they do not appear or disappear. The constant composition of compounds stems from the fact that the compounds consist of a definite ratio of atoms, each with a definite mass. The law of multiple proportions is due to the fact that different numbers of atoms of... [Pg.44]

The preparation of poly(m-carborane-siloxane) polymers has also been successfully achieved directly from the carborane monomer.22 The reaction used is shown in scheme 9. Here, the direct salt elimination reaction between dilithiocarborane and a dichlorosiloxane (e.g., 1,5-dichlorohexamethyltrisiloxane) results in the formation of linear polymers with a molecular-weight (M ) typically of 6800 dalton. However, the reported literature detailing this approach is very limited indeed, and the reaction has not found significant use. This is most probably because only relatively low molecular-weight polymers can be produced, ultimately restricting the flexibility to produce materials of controlled mechanical properties. [Pg.105]

Chatt, J. et al., J. Chem. Soc., Dalton Trans., 1985, 1131-1136 A modified method of preparation from ethylene, phosphorus trichloride and phosphorus in a stainless autoclave gives a highly pyrophoric reaction residue. [Pg.303]


See other pages where Dalton reaction is mentioned: [Pg.207]    [Pg.343]    [Pg.207]    [Pg.343]    [Pg.53]    [Pg.28]    [Pg.173]    [Pg.1048]    [Pg.313]    [Pg.716]    [Pg.466]    [Pg.366]    [Pg.7]    [Pg.201]    [Pg.986]    [Pg.81]    [Pg.89]    [Pg.277]    [Pg.333]    [Pg.803]    [Pg.21]    [Pg.127]    [Pg.77]    [Pg.464]    [Pg.258]    [Pg.181]    [Pg.361]   
See also in sourсe #XX -- [ Pg.73 ]




SEARCH



Dalton

© 2024 chempedia.info