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Bond angles pressure

Pressures used to investigate biochemical systems range from 0.1 MPa to 1 GPa (0.1 MPa = 1 bar 1 GPa == 10 kbar) such pressures only change intermolecular distances and afiect conformations but do not change covalent bond distances or bond angles. Pressures in excess of 30 GPa are required to change the electronic structure of a molecule. ... [Pg.116]

Linear molecule A triatomic molecule in which the bond angle is 180° examples include BeF2 and C02,176 Linear polyethylene, 612 Liquid scintillation counter, 518 Liquid-vapor equilibrium, 253-254q boiling point, 230-231 critical pressure, 231-232 critical temperature, 231-232 symbol, 227... [Pg.691]

Two modifications are known for polonium. At room temperature a-polonium is stable it has a cubic-primitive structure, every atom having an exact octahedral coordination (Fig. 2.4, p. 7). This is a rather unusual structure, but it also occurs for phosphorus and antimony at high pressures. At 54 °C a-Po is converted to /3-Po. The phase transition involves a compression in the direction of one of the body diagonals of the cubic-primitive unit cell, and the result is a rhombohedral lattice. The bond angles are 98.2°. [Pg.107]

Figure 8 Behavior of the first sharp diffraction peak of PB with experimental scattering lengths for carbon and deuterium. The deuterium atoms are placed at their mechanical equilibrium positions determined by the positions of the united atom centers and the equilibrium CH bond length and HCH and HCC bond angles along a united atom MD trajectory. With increasing pressure (values given in the legend, simulation performed at T = 293 K), the first sharp diffraction peak shifts to larger q as expected but unexpectedly decreases in height. Figure 8 Behavior of the first sharp diffraction peak of PB with experimental scattering lengths for carbon and deuterium. The deuterium atoms are placed at their mechanical equilibrium positions determined by the positions of the united atom centers and the equilibrium CH bond length and HCH and HCC bond angles along a united atom MD trajectory. With increasing pressure (values given in the legend, simulation performed at T = 293 K), the first sharp diffraction peak shifts to larger q as expected but unexpectedly decreases in height.
While the isomerization did not take place above 120°C, the usual boiling range of azoalkanes, it could be carried out at reduced pressure. It appears critical that a minimum amount of heat be applied to the system to cause refluxing by judicious use of low pressures and careful insulation of the apparatus. The method fails in an attempt to isomerize cyclooctanone methylhydrazone. The bond angle strain is said to effect the ease of rearrangement of the hydrazone... [Pg.421]

Disulfur monoxide, S20, can be prepared, along with SO, by the reduction of S02 in a glow discharge or from the reaction of metal sulfides with SOCl2. In the vapour phase at low pressure it slowly decomposes to S and S02 but in condensed phases it polymerizes. Its structure is similar to that of S02 with an SSO bond angle of 1 180.39 43 The complex t(Ph2PCH2CH2PPh2)2Ir(S20)]Cl (9) has been prepared by the reaction shown in equation (l).41 The complex (9) is air stable and the IR spectrum shows only one v(S—O) at 1043 cm-1.41,44 The complex [Mo(S20)(S2CNEt2)2] has also been isolated in small yield.45... [Pg.636]


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Pressure bonding

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