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Compatibility tetrahedrons

Fig. 4. The subsolidus phase relationships in the Si N SiC -AljCL-AlN-YjCL-YN system, showing compatibility tetrahedrons [J],... Fig. 4. The subsolidus phase relationships in the Si N SiC -AljCL-AlN-YjCL-YN system, showing compatibility tetrahedrons [J],...
Si3N4-Si02-AlN-Al203-YN-Y203 system determined by Naik and Tien [J] and Sun et al. [4]. Sixty-eight compatibility tetrahedrons in the Si-Al-Y-N-O system have been established by these authors. [Pg.131]

Fig. 22. Subsolidus phase relations in the Si,Al,Y/N, O system showing a series of compatibility tetrahedrons formed by a -sialon, j3 -SiA ON, and AIN polytypoids [34]. Fig. 22. Subsolidus phase relations in the Si,Al,Y/N, O system showing a series of compatibility tetrahedrons formed by a -sialon, j3 -SiA ON, and AIN polytypoids [34].
First we consider the geometry issues. As mentioned, only the hybridization compatible deformations of geometry affect the shape of the hybridization tetrahedron. On the other hand one can easily see that variation of the valence angle Xmm with m < m reduces to rotations of the involved bond vectors enmLm and around the axis orthogonal to the both coordination tetrahedron vectors ... [Pg.255]

The reaction of hybridization tetrahedron on the changes of local geometry can be considered in the linear response approximation eq. (3.133). It is clear that any variation of the valence angle is a sum of equal amounts of hybridization- compatible and hybridization- incompatible deformations. The denominator in the linear response relation eq. (3.133) is the same as for eq. (3.136) while the relevant block of the yxyqE matrix (with q taken as a difference of two opposite valence angles) is proportional to For the methane molecule with the carbon atom put in the origin of the coordinate frame, substitution of matrices of second derivatives for the energy... [Pg.255]

By integrating oh( ) up to the first minimum, a value of 1.92 was obtained. This means that each water molecule can form 3.84 hydrogen bonds with its first neighbours, a result compatible with a local structure of water at room temperature of four nearest molecules oriented in a tetrahedron configuration. [Pg.336]

Adinolfi, M, ladonisi. A, Schiattarella, M, An approach to the highly stereocontrolled synthesis of a-glycosides. Compatible use of the very acid labile dimethoxytrityl protecting group with Yb(OTf)3-promoted glycosidation. Tetrahedron Lett., 44, 6479-6482, 2003. [Pg.184]

Fig. 25 shows a compatibility relationships between oxynitride and /3-Si3N4. Note that the tetrahedron /3-Si3N4-/3-SiA10N-Y2Si207-Y3A15012 separates the silicon oxynitride from a -SiA10N and AIN... [Pg.153]

The Raman spectra of molten iron (III) chloride are best characterized as a structure, where neutral Fe2Cl6 and charged Fe2Cl and Fe2Cl7 are the predominant species. The Fe2Cl+ species compatible with the measured frequencies would consist of a FeCU tetrahedron bound by edge with a trigonal FeCb... [Pg.398]

A soln. of startg. thioglycoside in TFIF treated with 2 eqs. 1 M lithium naphthalenide in the same solvent at — 78°, stirred for a further 30 min after the disappearance of startg. m., and neutralized with 4 1 TFlF/acetic acid at —78° - product. Y 92%. The method is compatible with both acid- and base-labile protective groups. F.e. and from glycosyl sulfones s. A.Fernandez-Mayoralas et al.. Tetrahedron Letters 30, 2537 0 (1989). [Pg.198]

S. Shamim, I. R. Siddiqui, J. Heterocyclic Chem. 2013, 50, E111-E115. Ionic liquid promoted multicomponent reaction a good strategy for the eco-compatible synthesis of functionalized pyrroles, (f) B. M. Babu, G. S. Kumar, P. B. Thakur, V. M. Bangade, H. M. Meshram, Tetrahedron Lett. 2013, 54, 2296-2302. Catalyst-free four-component protocol for the synthesis of substituted pyrroles under reusable reaction media, (g) C. Martm-Santos, C. Jarava-Barrera, A. Parra, F. Esteban, C. Navarro-Ranninger, J. Alemin, ChemCatChem... [Pg.244]

Residual Ru species do not interfere with some subsequent transformations. Rodrigo B. Andrade of Temple University has demonstrated (Tetrahedron Lett. 2007, 48, 5367) that metathesis with an a, 3-unsaturated aldehyde such as 11 can be followed directly by phospho-nate condensation to give the doubly-homologated product 12. Philip 1. Parsons of the University of Sussex has found (Organic Lett. 2007, 9, 2613) that the nitro functional group is compatible with the Ru catalyst. The product nitro alkene 15 could be cychzed (intramolecular Michael addition) to the cyclopentane 16, or (intramolecular dipolar cycloaddition) to the cyclopentane 17. [Pg.46]

Chitkul B, Atrash B, Bradley M. A new bio-compatible pH cleavable linker for solid-phase synthesis of a squalamine analogue. Tetrahedron Lett. 2001 42 6211-6214. [Pg.116]


See other pages where Compatibility tetrahedrons is mentioned: [Pg.130]    [Pg.137]    [Pg.151]    [Pg.130]    [Pg.137]    [Pg.151]    [Pg.163]    [Pg.173]    [Pg.18]    [Pg.140]    [Pg.255]    [Pg.256]    [Pg.173]    [Pg.45]    [Pg.45]    [Pg.75]    [Pg.75]    [Pg.275]    [Pg.45]    [Pg.48]    [Pg.44]    [Pg.222]    [Pg.223]    [Pg.165]    [Pg.106]    [Pg.73]   
See also in sourсe #XX -- [ Pg.131 , Pg.137 ]




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