Big Chemical Encyclopedia

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

Articles Figures Tables About

Molecular dimension

X-ray analysis of an optically active oxaziridine substituted at nitrogen with the 1-phenylethyl group of known configuration led to the absolute configuration (+)-(2R,3R)-2-(5-l-phenylethyl)-3-(p-bromophenyl)oxaziridine of the dextrorotatory compound as expected, C-aryl and A-alkyl groups were trans to each other (79MI50800). [Pg.198]

Structural data of a diaziridine come from gas phase electron diffraction measurements (74CC397). The N—N bond of 3-methyldiaziridine (24) is longer than in hydrazine (1.449 A) the C—N bond distances in (24) and in diazirine are nearly equal (1.479 versus 1.482 A), [Pg.198]

X-ray analysis of diaziridinone (25) gave an N—N bond length of 1.60 A, and an N—CO bond length of 1.325 A. The bonds from nitrogen to substituent form angles of 56° with the plane of the ring the substituents are trans to each other (78JOC922). [Pg.199]

The molecular geometry of diazirine (3 R = H) was analyzed by microwave spectroscopy (62JA2651). Rotatory spectra of diazirine, of ( C)diazirine and of ( N- N)diazirine yielded the bond lengths and bond angles shown. The dipole moment of diazirine is 1.59 D. [Pg.199]

Bond lengths and bond angles of 3-methyldiazirine, 3,3-dimethyldiazirine, 3-chloro-3-methyldiazirine and 3-bromo-3-methyldiazirine were also obtained by microwave spectroscopy (70JCP(53)1543). [Pg.199]


This effect assumes importance only at very small radii, but it has some applications in the treatment of nucleation theory where the excess surface energy of small clusters is involved (see Section IX-2). An intrinsic difficulty with equations such as 111-20 is that the treatment, if not modelistic and hence partly empirical, assumes a continuous medium, yet the effect does not become important until curvature comparable to molecular dimensions is reached. Fisher and Israelachvili [24] measured the force due to the Laplace pressure for a pendular ring of liquid between crossed mica cylinders and concluded that for several organic liquids the effective surface tension remained unchanged... [Pg.54]

While most vesicles are formed from double-tail amphiphiles such as lipids, they can also be made from some single chain fatty acids [73], surfactant-cosurfactant mixtures [71], and bola (two-headed) amphiphiles [74]. In addition to the more common spherical shells, tubular vesicles have been observed in DMPC-alcohol mixtures [70]. Polymerizable lipids allow photo- or chemical polymerization that can sometimes stabilize the vesicle [65] however, the structural change in the bilayer on polymerization can cause giant vesicles to bud into smaller shells [76]. Multivesicular liposomes are collections of hundreds of bilayer enclosed water-filled compartments that are suitable for localized drug delivery [77]. The structures of these water-in-water vesicles resemble those of foams (see Section XIV-7) with the polyhedral structure persisting down to molecular dimensions as shown in Fig. XV-11. [Pg.549]

Adsorbents such as some silica gels and types of carbons and zeolites have pores of the order of molecular dimensions, that is, from several up to 10-15 A in diameter. Adsorption in such pores is not readily treated as a capillary condensation phenomenon—in fact, there is typically no hysteresis loop. What happens physically is that as multilayer adsorption develops, the pore becomes filled by a meeting of the adsorbed films from opposing walls. Pores showing this type of adsorption behavior have come to be called micropores—a conventional definition is that micropore diameters are of width not exceeding 20 A (larger pores are called mesopores), see Ref. 221a. [Pg.669]

In sunnnary, the SFA is a versatile instrument that represents a unique platfonu for many present and fiiture implementations. Unlike any other experimental teclmique, the SFA yields quantitative insight into molecular dimensions, structures and dynamics under confinement. [Pg.1738]

SInanojIu O 1981 Microscopic surface tension down to molecular dimensions and microthermodynamic surface areas of molecules or clusters J. Chem. Phys. 75 463—8... [Pg.2851]

These calculations lend theoretical support to the view arrived at earlier on phenomenological grounds, that adsorption in pores of molecular dimensions is sufficiently different from that in coarser pores to justify their assignment to a separate category as micropores. The calculations further indicate that the upper limit of size at which a pore begins to function as a micropore depends on the diameter a of the adsorbate molecule for slit-like pores this limit will lie at a width around I-So, but for pores which approximate to the cylindrical model it lies at a pore diameter around 2 5(t. The exact value of the limit will of course depend on the actual shape of the pore, and may well be raised by cooperative effects. [Pg.209]

If a Type I isotherm exhibits a nearly constant adsorption at high relative pressure, the micropore volume is given by the amount adsorbed (converted to a liquid volume) in the plateau region, since the mesopore volume and the external surface are both relatively small. In the more usual case where the Type I isotherm has a finite slope at high relative pressures, both the external area and the micropore volume can be evaluated by the a,-method provided that a standard isotherm on a suitable non-porous reference solid is available. Alternatively, the nonane pre-adsorption method may be used in appropriate cases to separate the processes of micropore filling and surface coverage. At present, however, there is no reliable procedure for the computation of micropore size distribution from a single isotherm but if the size extends down to micropores of molecular dimensions, adsorptive molecules of selected size can be employed as molecular probes. [Pg.286]

In earlier chapters an unperturbed coil referred to molecular dimensions as predicted by random flight statistics. We saw in the last chapter that this thermodynamic criterion is met under 0 conditions. [Pg.614]

The chemical effects of ultrasound do not arise from a direct interaction with molecular species. Ultrasound spans the frequencies of roughly 15 kH2 to 1 GH2. With sound velocities in Hquids typically about 1500 m/s, acoustic wavelengths range from roughly 10 to lO " cm. These are not molecular dimensions. Consequently, no direct coupling of the acoustic field with chemical species on a molecular level can account for sonochemistry or sonoluminescence. [Pg.255]

Fig. 7. Molecular dimension and 2eohte pore si2e. Chart showing a correlation between effective pore si2e of various 2eohtes over temperatures of 77—420 K (-----------------) with the kinetic diameters of various molecules (1). M—A is a cation—2eohte A system. M—X is a cation—2eohte X system. Fig. 7. Molecular dimension and 2eohte pore si2e. Chart showing a correlation between effective pore si2e of various 2eohtes over temperatures of 77—420 K (-----------------) with the kinetic diameters of various molecules (1). M—A is a cation—2eohte A system. M—X is a cation—2eohte X system.
Many of the unique properties of siUcone oils are associated with the surface effects of dimethylsiloxanes, eg, imparting water repeUency to fabrics, antifoaming agents, release liners for adhesive labels, and a variety of poHshes and waxes (343). Dimethylsilicone oils can spread onto many soHd and Hquid surfaces to form films of molecular dimensions (344,345). This phenomenon is greatly affected by even small changes in the chemical stmcture of siloxane in the siloxane polymer. Increasing the size of the alkyl substituent from methyl to ethyl dramatically reduces the film-forming abiUty of the polymer (346). The phenyl-substituted siUcones are spread onto water or soHd surfaces more slowly than PDMS (347). [Pg.52]

Dj IE, ratio of a crack is held constant but the dimensions approach molecular dimensions, the crack becomes more retentive. At room temperature, gaseous molecules can enter such a crack direcdy and by two-dimensional diffusion processes. The amount of work necessary to remove completely the water from the pores of an artificial 2eohte can be as high as 400 kj/mol (95.6 kcal/mol). The reason is that the water molecule can make up to six H-bond attachments to the walls of a pore when the pore size is only slightly larger. In comparison, the heat of vaporization of bulk water is 42 kJ /mol (10 kcal/mol), and the heat of desorption of submonolayer water molecules on a plane, soHd substrate is up to 59 kJ/mol (14.1 kcal/mol). The heat of desorption appears as a exponential in the equation correlating desorption rate and temperature (see Molecularsieves). [Pg.369]

Electrically, the electrical double layer may be viewed as a capacitor with the charges separated by a distance of the order of molecular dimensions. The measured capacitance ranges from about two to several hundred microfarads per square centimeter depending on the stmcture of the double layer, the potential, and the composition of the electrode materials. Figure 4 illustrates the behavior of the capacitance and potential for a mercury electrode where the double layer capacitance is about 16 p.F/cm when cations occupy the OHP and about 38 p.F/cm when anions occupy the IHP. The behavior of other electrode materials is judged to be similar. [Pg.511]

These tetrahedra are arranged in a number of ways to give the different zeohtes. The stmctures are unique in that they incorporate pores as part of the regular crystalline stmctures. The pores have dimensions of the order of molecular dimensions so that some molecules fit into the pores and some do not. Hence the zeohtes are molecular sieves (qv), and they are apphed in industrial separations processes to take advantage of this property. Some zeohtes and their pore dimensions are hsted in Table 2. [Pg.177]

Figure 2 Molecular dimensions and dipole moments of some simple azines... Figure 2 Molecular dimensions and dipole moments of some simple azines...
High accuracy molecular dimensions for the planar parent heterocycles in the gas phase have been obtained by microwave spectroscopy and are recorded in Table 2. These values have been corroborated for furan by a low-temperature X-ray crystallographic study... [Pg.3]

Theoretical and structural studies have been briefly reviewed as late as 1979 (79AHC(25)147) (discussed were the aromaticity, basicity, thermodynamic properties, molecular dimensions and tautomeric properties ) and also in the early 1960s (63ahC(2)365, 62hC(17)1, p. 117). Significant new data have not been added but refinements in the data have been recorded. Tables on electron density, density, refractive indexes, molar refractivity, surface data and dissociation constants of isoxazole and its derivatives have been compiled (62HC(17)l,p. 177). Short reviews on all aspects of the physical properties as applied to isoxazoles have appeared in the series Physical Methods in Heterocyclic Chemistry (1963-1976, vols. 1-6). [Pg.3]

Benzotriazolium tetrachlorocobaltates crystal structure, 5, 676 Benzotrifuroxans molecular dimensions, 6, 397 N NMR, 6, 398 photoelectron spectra, 6, 399 Benzotropones synthesis, 2, 308 2H-Benz[e][l,2]oxaborins benzo fused synthesis, 1, 659 synthesis, 1, 659... [Pg.565]

Chroman-2-ylmethanol, (5)-6-hydroxy-2,5,7,8-tetramethyl-synthesis, 3, 779 Chromene, 3-acetyl-2-methoxy-synthesis, 3, 750 Chromene, 2-alkyl-synthesis, 3, 749 Chromene, 4-aryloxymethyl-synthesis, 3, 742-743 Chromene, bis(2,2-dimethyl-mass spectra, 3, 604 Chromene, 2,3-dichloro-synthesis, 3, 753 Chromene, 2,2-dimethyl-IR spectra, 3, 594 mass Spectra, 3, 604 molecular dimensions, 3, 621 synthesis, 3, 743, 749, 751 Chromene, 3-fluoro-2,2-dimethyl-synthesis, 3, 748 Chromene, 5-hydroxy-synthesis, 3, 745... [Pg.580]

Dithienobenzene synthesis, 4, 720 Dithieno[3,2-fc 2,3-/]borepin molecular dimensions, 1, 633 Dithienoborepins stability, 1, 660... [Pg.614]


See other pages where Molecular dimension is mentioned: [Pg.262]    [Pg.113]    [Pg.243]    [Pg.377]    [Pg.456]    [Pg.466]    [Pg.222]    [Pg.648]    [Pg.2388]    [Pg.2609]    [Pg.2789]    [Pg.204]    [Pg.235]    [Pg.694]    [Pg.417]    [Pg.251]    [Pg.72]    [Pg.448]    [Pg.162]    [Pg.194]    [Pg.196]    [Pg.21]    [Pg.4]    [Pg.198]    [Pg.545]    [Pg.549]    [Pg.550]    [Pg.555]    [Pg.571]   
See also in sourсe #XX -- [ Pg.304 , Pg.307 , Pg.308 ]

See also in sourсe #XX -- [ Pg.274 ]

See also in sourсe #XX -- [ Pg.180 , Pg.209 ]

See also in sourсe #XX -- [ Pg.46 ]

See also in sourсe #XX -- [ Pg.34 ]

See also in sourсe #XX -- [ Pg.2 , Pg.323 , Pg.324 , Pg.325 , Pg.326 , Pg.327 , Pg.328 , Pg.329 , Pg.330 , Pg.331 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.3 , Pg.5 , Pg.154 , Pg.858 ]

See also in sourсe #XX -- [ Pg.25 ]

See also in sourсe #XX -- [ Pg.2 , Pg.323 , Pg.324 , Pg.325 , Pg.326 , Pg.327 , Pg.328 , Pg.329 , Pg.330 , Pg.331 ]

See also in sourсe #XX -- [ Pg.80 ]

See also in sourсe #XX -- [ Pg.303 , Pg.306 ]




SEARCH



Amorphous state molecular dimensions

Benzene molecular dimensions

Changes in molecular dimensions

Critical molecular dimensions

Critical molecular dimensions zeolites

Crystalline state molecular dimensions

Determination of Polymer Molecular Dimensions from Viscosity

Dimensions, direct determination molecular

Direct Determination of Molecular Dimensions

Displacement length Molecular dimensions)

Folded proteins, molecular dimension

Molecular dimensions average values

Molecular dimensions from light scattering

Molecular dimensions length)

Molecular dimensions optimized

Molecular dimensions unperturbed

Molecular dimensions viscosity

Molecular dimensions, direct

Molecular dimensions, reviews

Molecular dimensions, water molecule

Molecular dynamics four dimensions

Molecular pore dimensions

Molecular surface pore dimension

Molecular three dimensioned

Molecular weight dimensions

Plasma proteins molecular dimensions

Pyridines molecular dimensions

Refractivity and Atomic or Molecular Dimensions

Structure and molecular dimensions

The Determination of Molecular Dimensions

The Time Dimension Molecular Dynamics

Three dimension molecular descriptors

Toluene molecular dimensions

Water molecular dimensions

Water, properties molecular dimension

© 2024 chempedia.info