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Hydrogen rupture

Fig. 6. Force profile obtained from a one nanosecond simulation of streptavidin-biotin rupture showing a series of subsequent force peaks most of these can be related to the rupture of individual microscopic interactions such as hydrogen bonds (bold dashed lines indicate their time of rupture) or water bridges (thin dashed lines). Fig. 6. Force profile obtained from a one nanosecond simulation of streptavidin-biotin rupture showing a series of subsequent force peaks most of these can be related to the rupture of individual microscopic interactions such as hydrogen bonds (bold dashed lines indicate their time of rupture) or water bridges (thin dashed lines).
Fig. 7. Snapshots of rupture taken (A) at the start of the simulation (zcant = 0), (li) at ZcB.nl = 2.8 A, (C) at Zcnm = 4.1 A, (D) at Zcnm = 7.1 A, and (E) at Zcant = 10.5 A. The biotin molecule is drawn as a ball-and-stick model within the binding )ocket (lines). The bold dashed lines show hydrogen bonds, the dotted lines show selected water bridges. Fig. 7. Snapshots of rupture taken (A) at the start of the simulation (zcant = 0), (li) at ZcB.nl = 2.8 A, (C) at Zcnm = 4.1 A, (D) at Zcnm = 7.1 A, and (E) at Zcant = 10.5 A. The biotin molecule is drawn as a ball-and-stick model within the binding )ocket (lines). The bold dashed lines show hydrogen bonds, the dotted lines show selected water bridges.
Rupture by hydrogen iodide. Ethers are usually broken up by hot hydrogen iodide thus ... [Pg.397]

Fire Hazards - Flash Point (deg. F) 252 OC Flammable Limits in Air (%) Not pertinent Fire Extinguishing Agents Water Fire Extinguishing Agents Not To Be Used Not pertinent Special Hazards of Combustion Products Toxic fumes include oxides of phosphorous, sulfur and hydrogen chloride Behavior in Fire Containers may rupture Ignition Temperature (deg. F) 338 Electrical Hazard No data Burning Rate No data. [Pg.40]

Small and Browning agree with Schbpf and Winterhalder that thebainone methyl enolate (formed by 1 6 addition in which the oxygen bridge is ruptured and ethylenic linkages produced at C —C and C —C ) may be the primary intermediate in tWs reaction since it is hydrogenated... [Pg.242]

The acetoxy dienone (218) gives phenol (220). Here, an alternative primary photoreaction competes effectively with the dienone 1,5-bonding expulsion of the lOjS-acetoxy substituent and hydrogen uptake from the solvent (dioxane). In the case of the hydroxy analog (219) the two paths are balanced and products from both processes, phenol (220) and diketone (222), are isolated. In the formation of the spiro compound (222) rupture of the 1,10-bond in the dipolar intermediate (221) predominates over the normal electron transmission in aprotic solvents from the enolate moiety via the three-membered ring to the electron-deficient carbon. While in protic solvents and in 10-methyl compounds this process is inhibited by the protonation of the enolate system in the dipolar intermediate [cf. (202), (203)], proton elimination from the tertiary hydroxy group in (221) could reverse the efficiencies of the two oxygens as electron sources. [Pg.335]

The build-up of calcareous deposits is a complex topic. Very high current densities will not necessarily result in the most protective scale. In the extreme, hydrogen evolution may rupture the scale resulting in reduced protection. An optimum current density will exist, and this should be recognised. [Pg.159]

Hydrogen embrittlement (hydrogen damage) Only in boilers over 1000 psig, leading to violent tube rupture. [Pg.272]


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See also in sourсe #XX -- [ Pg.146 ]




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