Big Chemical Encyclopedia

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

Articles Figures Tables About

Brady bonds

We have deleted the chapters on cubic spline (a technique now very well known and with plenty of material about it out there on the internet) and Brady bonds. We have also removed the earlier edition s chapters on risk-free sovereign bonds trading, oti the grounds that the logic of analysis employed for such investments has not changed since 2003, and also more indirectly because there are so few genuinely risk-free sovereign issuers left in the world ... [Pg.248]

Credit derivative products are defined by reference to underlying reference entities, and reference obligations, which include corporate bonds, bank loans, sovereign debt, Brady bonds, and Eurobonds. Credit derivatives are now used increasingly in structured transactions. For example synthetic collateralised loan obligations (see Chapter 15) often use credit default swaps to transfer credit risk from the originator to the special purpose vehicle (SPV). Currently, the most common products are credit default products and total return swaps. [Pg.654]

Brady bond U S. dollar-denominated bond issued by an emerging market, particularly those in Latin America, and collateralized by U S. Treasury zero-... [Pg.165]

The hydrogenolyaia of cyclopropane rings (C—C bond cleavage) has been described on p, 105. In syntheses of complex molecules reductive cleavage of alcohols, epoxides, and enol ethers of 5-keto esters are the most important examples, and some selectivity rules will be given. Primary alcohols are converted into tosylates much faster than secondary alcohols. The tosylate group is substituted by hydrogen upon treatment with LiAlH (W. Zorbach, 1961). Epoxides are also easily opened by LiAlH. The hydride ion attacks the less hindered carbon atom of the epoxide (H.B. Henhest, 1956). The reduction of sterically hindered enol ethers of 9-keto esters with lithium in ammonia leads to the a,/S-unsaturated ester and subsequently to the saturated ester in reasonable yields (R.M. Coates, 1970). Tributyltin hydride reduces halides to hydrocarbons stereoselectively in a free-radical chain reaction (L.W. Menapace, 1964) and reacts only slowly with C 0 and C—C double bonds (W.T. Brady, 1970 H.G. Kuivila, 1968). [Pg.114]

Otner Collectors Tarry particulates and other difficult-to-handle hquids have been collected on a dry, expendable phenol formaldehyde-bonded glass-fiber mat (Goldfield, J. Air Pollut. Control A.SSOC., 20, 466 (1970)] in roll form which is advanced intermittently into a filter frame. Superficial gas velocities are 2.5 to 3.5 m/s (8.2 to 11.5 ft/s), and pressure drop is typically 41 to 46 cm (16 to 18 in) of water. CoUection efficiencies of 99 percent have been obtained on submicrometer particles. Brady [Chem. Eng. Prog., 73(8), 45 (1977)] has discussed a cleanable modification of this approach in which the gas is passed through a reticulated foam filter that is slowly rotated and solvent-cleaned. [Pg.1441]

Fig. 2 Gradient separation of peptide mixture on a C30 bonded phase. Mobile phase, linear gradient from 25% to 45% A in 15 min. A = 0.1% trifluoroacetic acid (TFA) in 75 25 acetonitrile-water and B = 0.1% TFA in water. Solutes 1 = brady-kinin 2 = angiotensin III 3 = angiotensin I. Fig. 2 Gradient separation of peptide mixture on a C30 bonded phase. Mobile phase, linear gradient from 25% to 45% A in 15 min. A = 0.1% trifluoroacetic acid (TFA) in 75 25 acetonitrile-water and B = 0.1% TFA in water. Solutes 1 = brady-kinin 2 = angiotensin III 3 = angiotensin I.
J. W. Brady and R. K. Schmidt, /. Phys. Chem., 97, 958 (1993). The Role of Hydrogen Bonding in Carbohydrates Molecular Dynamics Simulations of Maltose in Aqueous Solu-... [Pg.163]

Fig. 19.8. A proposed secondary strucmre of Fe403(0H)4(N03)2 I.5H2O shown as a projection on the plane of the paper. The vectors a and h are the probable Fe-Fe interactions corresponding to the two peaks at 5.6 and 6.4 A in the radial distribution function. The NOj ions are thought to be hydrogen bonded to the HjO molecules on the surface. (Brady et ai, 1968.)... Fig. 19.8. A proposed secondary strucmre of Fe403(0H)4(N03)2 I.5H2O shown as a projection on the plane of the paper. The vectors a and h are the probable Fe-Fe interactions corresponding to the two peaks at 5.6 and 6.4 A in the radial distribution function. The NOj ions are thought to be hydrogen bonded to the HjO molecules on the surface. (Brady et ai, 1968.)...
The mechanism is very complicated, as more than 36 reactions have been proposed. " Illustrated here is a simple demonstration of this reaction, where iron is used to indicate the catalytic center only, no other bonds are shown except for the necessary ones. This mechanism is similar to the one in Brady and Pettit. [Pg.1099]


See other pages where Brady bonds is mentioned: [Pg.209]    [Pg.233]    [Pg.209]    [Pg.249]    [Pg.21]    [Pg.175]    [Pg.338]    [Pg.88]    [Pg.232]    [Pg.314]    [Pg.4]    [Pg.168]    [Pg.268]    [Pg.269]    [Pg.259]    [Pg.358]    [Pg.705]    [Pg.114]    [Pg.1723]    [Pg.246]    [Pg.328]    [Pg.85]    [Pg.156]    [Pg.388]    [Pg.318]    [Pg.159]    [Pg.124]    [Pg.64]    [Pg.484]    [Pg.486]    [Pg.866]    [Pg.726]    [Pg.142]   
See also in sourсe #XX -- [ Pg.654 ]




SEARCH



Brady

© 2024 chempedia.info