Big Chemical Encyclopedia

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

Articles Figures Tables About

Dunitz

M. Dunitz, M A.tlas of the Musmkskektal System, CRC Press, Boca Raton, Fla., 1989. [Pg.59]

G. J. Mount, in The Clinician s Handbook, Martin Dunitz, London, 1989. [Pg.496]

Results of quantum-mechanical calculations (Dunitz and Orgel, 1957) have given values for the OSPEs of a number of transitional metal ions and the degree of inversion of mixed spinels... [Pg.238]

Prof. Dr. Jack D. Dunitz Laboratorium fur Organische Chemie der Eidgenossischen Hochschule UniversitatsslraBe 6/8, CH-8006 Zurich... [Pg.153]

Wallis and Dunitz (1984a) also investigated another type of sterically induced interaction of a donor group with a diazonio group. Quinoline-8-diazonium-l-oxide tetrafluoroborate (4.14) was analyzed at 95 K (R = 0.034). [Pg.73]

Fig. 4-1. Distances (pm) and angles (°) relevant to the 0(1) N(l) = N(2) interaction in the quino-line-8-diazonium-l-oxide ion 4.14 (after Wallis and Dunitz, 1984 a). Fig. 4-1. Distances (pm) and angles (°) relevant to the 0(1) N(l) = N(2) interaction in the quino-line-8-diazonium-l-oxide ion 4.14 (after Wallis and Dunitz, 1984 a).
The structure of 1,2,3-benzoxadiazole (4.16) bears some resemblance to Wallis and Dunitz s structure (4.14, Fig. 4-1) for quinoline-8-diazonium-l-oxide, as the latter structure has a tendency towards forming a five-membered heteroaromatic ring. The two compounds are, however, different with respect to the involvement of an N(2) and an N(l) diazo atom. The 1,2,3-benzoxadiazole structure is consistent with the bands observed in the 9.45 to 12.37 eV range in the photoelectron spectrum,... [Pg.74]

Atom numbering as in Figure 11-1.1 thank my colleague J. D. Dunitz (ETH Zurich) for providing the appropriate computer program for the calculation of these atomic distances and the various N O distances mentioned below. [Pg.292]

Dunitz, J. D. (1979) X-Ray Analysis and the Structure of Organic Molecules. Cornell University Press, Ithaca NY [4.2]. [Pg.415]


See other pages where Dunitz is mentioned: [Pg.92]    [Pg.40]    [Pg.363]    [Pg.490]    [Pg.173]    [Pg.86]    [Pg.148]    [Pg.436]    [Pg.436]    [Pg.518]    [Pg.793]    [Pg.314]    [Pg.330]    [Pg.937]    [Pg.217]    [Pg.172]    [Pg.996]    [Pg.218]    [Pg.130]    [Pg.136]    [Pg.247]    [Pg.377]    [Pg.787]    [Pg.655]    [Pg.6]    [Pg.187]    [Pg.513]    [Pg.513]    [Pg.85]    [Pg.66]    [Pg.71]    [Pg.74]    [Pg.125]    [Pg.155]    [Pg.387]    [Pg.410]    [Pg.411]    [Pg.411]    [Pg.443]    [Pg.443]    [Pg.443]    [Pg.443]   
See also in sourсe #XX -- [ Pg.465 ]

See also in sourсe #XX -- [ Pg.32 , Pg.64 ]

See also in sourсe #XX -- [ Pg.230 ]

See also in sourсe #XX -- [ Pg.198 ]




SEARCH



Biirgi-Dunitz angle

Biirgi-Dunitz trajectory

Btirgi-Dunitz trajectory

Btlrgi-Dunitz trajectory

Burgi-Dunitz angle

Burgi-Dunitz trajectory

Dunitz angle

Dunitz, Jack

Dunitz-Burgi attack

Jack D. Dunitz

Stereochemistry of Ionic Solids J. D. Dunitz and L. E. Orgel

The Biirgi-Dunitz Angle

Thoughts on Crystals as Supermolecules Dunitz)

Winkler-Dunitz distortion parameters

© 2024 chempedia.info