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CD structure

Compact dendritic (CD) structures formally exist at arbitrarily small anisotropy e but their velocity goes to zero with e 0. It was only recently discovered that there is another structure, compact seaweed (CS), which is favorable for smaller e and larger A [94]. [Pg.892]

A similar one-step process was employed successfully [66] to prepare well-crystallized CdS thin films of optical quality on Au(lll) from an aqueous solution of CdSOa, EDTA, and Na2S at room temperature. A phase transition from cubic (zinc blende) to hexagonal (wurtzite) CdS structure was observed with decreasing pH below 5, while highly preferential orientation along [11.0] directions for the... [Pg.168]

Tomasi, J. (1994) Application of continuum solvation models based on a Quantum Mechanical Hamiltonian.,in Cramer, C. J. and Truhlar, D. ( .(cds.). Structure and Reactivity in Aqueous Solution, American Chemical Society, Washington,pp. 10-23. [Pg.348]

White 1993, Plastic Hinge Based Methods for advanced Analysis and Design of Steel Frames, D. W. White and W. F. Chen (cds), Structural Stability Research Council, Lehigh University, Bethlehem, Pennsylvania, 1993... [Pg.133]

UPD Cd can also be used to obtain cadmium sulfide, an important semiconductor for electronics. Electrochemical epitaxial growth of organized CdS structures, involving underpotentially deposited Cd on Au(lll) was thus reported [161, 265]. [Pg.784]

From 1975 to 1990, scientists at the University of Kansas utilized a rational synthetic design for the definition of a new excipient, the SBE derivative of P-CD (SBE7-P-CD CAPTISOL ). Designing renal safety into the CD was approached by introducing anionic substituents onto the CD structure. This approach capitalized on the increased water solubility that would be realized with the introduction of an ionic substituent. Higher intrinsic water solubility was expected to help minimize the potential precipitation of the CD, if concentrated in the kidney cell, and the charged substituent was expected to capitalize on the ability of the kidney to efficiently excrete ionic compounds into the urine, thus reducing residence time and exposure of the kidney cells to the CD. [Pg.60]

In the last family, the sulfonate anion is attached to a neutral alkyl spacer unit [-(CH2) -, where n = 2 to 6] that links to the CD structure by a metabolically stable ether linkage. This group of compounds differs from the first two families in that the anionic charge is spaced away from the carbohydrate backbone by the alkyl group. [Pg.61]

FIGURE 1 Schematic representation of natural CD structure and modification sites. [Pg.1227]

Application Advanced technology to produce high-purity cumene from propylene and benzene using patented catalytic distillation (CD) technology. The CDCumene process uses a specially formulated zeolite alkylation catalyst packaged in a proprietary CD structure and another specially formulated zeolite transalkylation catalyst in loose form. [Pg.47]

Kniewel R., Buglino JA., Shen V, Chadha T., Beckwith A., Lima CD. Structural analysis of Saccharomyces cerevisiae myo-inositol phosphate synthase. J Struct Fund Genomics. 2002 2(3) 129-34. [Pg.338]

Ultraviolet (UV) spectroscopy is a method cd structure determination applicable specifically to conjugated systems. When a coi jugated molecule is irradiated with ultraviolet light, ener gy absorption occurs and a it electron is promoted from the highest occupied molecular orbital tHOMOl to the lowest unoccupied molecular orbital (L.UMO1. For I,3< butadiene, radiation of 217 nm ia required. As a general rule, the... [Pg.571]

Much more attention has been paid to ring C. Trost and Fray reported an enantiomerically pure access to such a fragment in the course of their efforts toward taxanes (108). The CD structural element of taxol has been treated by several groups. Clark and co-workers (107,109) constructed oxetane 140 by substitution of a primary mesylate. [Pg.229]

In 1980 it was pointed out that the prolamellar body is a perfect example of a Cp structure [4]. (Later, more detailed, analyses have revealed that it may also be a Cd structure cf. section 7.2.) Following work on the structure of cubic phases, it was also realised that two-dimensional analogues are possible. This in turn suggested that a phase transition involving changes in the intrinsic curvature of membranes might be possible [29, 30]. Such a mechanism has far reaching implications. Clear evidence for such transitions between bilayer conformations has been reported [9]. This membrane bilayer model will be described below. [Pg.215]

As expected, adding the contribution from the impurity phase (again as Le Bail s approximation) results in further reduction of the profile residuals, see row six in Table 7.7. The final model of this crystal structure, as determined using the combined Rietveld refinement in the two-phase approximation, is found in the data file Ch7Ex01k.inp on the CD. Structural parameters are listed in Table 7.8. [Pg.626]

Dixon RA, Sigal IS, Strader CD. Structure-function analysis of the p-adrenergic receptor. Cold Spring Harb Symp Quant Biol 1988 53 Pt 1 487-497. [Pg.68]

Glaser, R. W., Grime, M., Wandelt, C. and Ulrich, A. S. (1999) NMR and CD structural analysis of the fusogenic peptide sequence B18 from the fertilization protein bindin. Biochemistry, 38, 2560-2569. [Pg.493]

Wester MR, Johnson EF, Marques-Soares C, Dansette PM, Mansuy D, Stout CD. Structure of a substrate complex of mammalian cytochrome P450 2C5 at 2.3 A resolution Evidence for multiple substrate binding modes. Biochemistry 2003 42 6370-9. [Pg.459]

Zhao Y, White MA, Muralidhara BK, Sun L, Halpert JR, Stout CD. Structure of microsomal cytochrome P450 2B4 complexed with the antifungal drug bifon-azole Insight into P450 conformational plasticity and membrane interaction. J Biol Chem 2006 281 5973-81. [Pg.512]

A schematic of a CD process for cumene production is shown in Fig. 3. The CDTECH process uses a zeolite catalyst in one of its patented CD structures and the product yield exceeds 99.5% purity with 99.9% selectivity to cumene. The high selectivity to cumene is achieved by controlling a low propylene concentration in the reaction section using a combination of process parameters such as system pressure, location of catalyst zone, and feedpoint. A low propylene concentration will result in a low propylene oligomerization rate and hence will reduce the amount of diisopropylbenzene and triisopropylbenzene produced by the consecutive reactions. One interesting aspect of this process is to recycle the diisopropylbenzene and triisopropyl benzene where transalkylation with benzene produces more cumene. [Pg.2603]

Chen X-S, Funk CD. Structure-function properties of human platelet 12-lipoxygenase Chimeric enzyme and in vitro mutagenesis studies. FASEB J. 7 (1993) 694-701. [Pg.161]


See other pages where CD structure is mentioned: [Pg.894]    [Pg.187]    [Pg.261]    [Pg.214]    [Pg.159]    [Pg.787]    [Pg.788]    [Pg.168]    [Pg.169]    [Pg.495]    [Pg.496]    [Pg.535]    [Pg.538]    [Pg.675]    [Pg.683]    [Pg.204]    [Pg.204]    [Pg.1899]    [Pg.787]    [Pg.788]    [Pg.361]    [Pg.339]    [Pg.203]    [Pg.207]   
See also in sourсe #XX -- [ Pg.11 , Pg.567 ]




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Structure of Paracoccus pantotrophus Cytochrome cd

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