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Related Donors

Imidazole and Related Donors. Structural models for the co-ordination geometries of a Cu-Cu redox couple in copper enzymes suggest a mechanism for where both electrons and protons are involved a model has been characterized bis(imidazole) copper(ii) diacetate (102). Dark green crystals of [Cu(caffeine)Cl2,H20] in which copper is tetragonal pyramidal distorted towards trigonal bipyramidal have been characterized Cu—Ni = 1.98 A,Cu—0(H20) = 1.96 A, Cu—Cl = 2.32,2.25 A. Dinitrato-2,6-bis-[l-(phenylimino)ethyl]pyridinecopper(ii) (103) contains a planar [Pg.280]


Lippert E, Ayuk AA, Rettig W, Wermuth G (1981) Adiabatic photoreactions in dilute solutions of p-substituted N, N -dialkylanilines and related donor-acceptor compounds. J Photochem 17 237-241... [Pg.303]

Except for very electron-rich donors that yield stable, persistent radical cations, the ox values are not generally available.64 Thus the cation radicals for most organic donors are too reactive to allow the measurement of their reversible oxidation potentials in either aqueous (or most organic) solvents by the standard techniques.65 This problem is partially alleviated by the measurement of the irreversible anodic peak potentials E that are readily obtained from the linear sweep or cyclic voltammograms (CV). Since the values of E contain contributions from kinetic terms, comparison with the values of the thermodynamic E is necessarily restricted to a series of structurally related donors,66 i.e.,... [Pg.219]

The quantitative treatment of the electron-transfer paradigm in Scheme l by FERET (equation (104)) is restricted to the comparative study of a series of structurally related donors (or acceptors). Under these conditions, the reactivity differences due to electronic properties inherent to the donor (or acceptor) are the dominant factors in the charge-transfer assessment, and any differences due to steric effects are considered minor. Such a situation is sufficient to demonstrate the viability of the electron-transfer paradigm to a specific type of donor acceptor behavior (e.g. aromatic substitution, olefin addition, etc.). However, a more general consideration requires that any steric effect be directly addressed. [Pg.301]

Outer-Sphere Electron Transfer The minimal interpenetration of the coordination spheres of the reactants is inherent in any mechanistic formulation of the outer-sphere process for electron transfer. As such, steric effects provide a basic experimental criterion to establish this mechanism. Therefore we wish to employ the series of structurally related donors possessing the finely graded steric and polar properties described in the foregoing section for the study of both homogeneous and heterogeneous processes for electron transfer. [Pg.115]

Linear triatomic anions The pioneering crystallographic studies of Odd Hassel140 on trihalides and related donor-acceptor species led to a far-reaching analysis of such Hassel compounds by Henry Bent.141 The triiodide ion (I3-, stable in aqueous solution) and other known linear trihalide XYZ- species also served as the prototype for Pimentel s incisive three-center MO analysis of hypervalency. We shall therefore begin with NBO/NRT investigation of a series of hypervalent and non-hypervalent triatomic anions in order to make contact with these classic studies. While ab initio studies add many quantitative details to the understanding of these species, the basic picture sketched by Bent and Pimentel is found to be essentially preserved. [Pg.286]

Hydroxyapatite constitutes -65% of human bone by weight. There is another 18% collagen fiber which makes the bone flexible and more durable. Then, there is -10% genetic tissue (mostly living bone cells). This tissue carries the genetic code of the person or animal and unless it is in a denatured form, which also kills the bone, it is likely to be rejected in the body as a bone graft. Therefore, it is impossible to successfully implant living bone even from closely related donors. The remainder of bone is composed of capillaries, nerves, and so on. [Pg.317]

Bone-marrow transplantation from siblings or compatible non-related donors has also proved useful in CGD treatment. The possibility also exists... [Pg.271]

The service for searching of the HLA-compatible non-related donors abroad in the international banks of bone marrow donors is not still created in Ukraine therefore, the Ukrainian transplantation centers today do not have the possibility to carry out the search of donors abroad for performing bone marrow transplantations in Ukraine. [Pg.260]

Beatty PG, Glift RA, Mickelson EM, Nisperos BB, Flournoy N, Martin PJ, Sanders JE, Stewart P, Buckner GD, Storb R. Marrow transplantation from related donors other than HLA identical siblings. N Engl J Med. 1985 Sep 26 313(13) 765 71. [Pg.273]

In most patients who develop CRF, renal transplantation from cadaver donors or living related donors is desirable. Post-transplant immuno-suppression with calcineurin inhibitors (e.g. cyclosporin, tacrolimus), anti-proliferative agents (e.g. azathioprine, myco-phenolate mofetil) and steroids (prednisolone), singly or in combination, are required. It has been... [Pg.611]

In our review, we distinguished two types of DNA-related donor-acceptor systems models where donor and acceptor interact directly, and models where they are separated by intervening base pairs. [Pg.65]

Lee, S.T., Jang, J. H., Cheong, J. W., et al. (2002),Treatment of high-risk acute myelogenous leukaemia by myeloablative chemoradiotherapy followed by co-infusion of T cell-depleted haematopoietic stem cells and culture-expanded marrow mesenchymal stem cells from a related donor with one fully mismatched human leucocyte antigen haplotype, Br. J. Haematol, 118(4), 1128-1131. [Pg.113]

Figure 2.3 Elements displaying soft acid or soft base behavior as donor or acceptor atoms in their compounds (heavy shading). Elements shown in light shading are borderline soft carbon is soft in CN, CO, and related donor molecules. Unshaded elements are hard. Heavy line encloses bases. Figure 2.3 Elements displaying soft acid or soft base behavior as donor or acceptor atoms in their compounds (heavy shading). Elements shown in light shading are borderline soft carbon is soft in CN, CO, and related donor molecules. Unshaded elements are hard. Heavy line encloses bases.
Marrow transplantation from related donors other than HLA-identical siblings Beatty, P.G., Clift, R.A., Mickelson, E.M., Nisperos, B.B., Flournoy, N., Martin, P.J.,... [Pg.74]

Takizawa D, Sato E, Hiraoka H, et al. Changes in apparent systemic clearance of propofol during transplantation of living related donor liver. Br J Anaesth 2005 95 (5) 643-647. [Pg.117]

Bunin N, Aplenc R, Leahey A, Magira E, Grupp S, Pierson G, Monos D. Outcomes of transplantation with partial T-cell depletion of matched or mismatched unrelated or partially matched related donor bone marrow in children and adolescents with leukemias. Bone Marrow Transplant 2005 35 151-8. [Pg.239]

Use of the complexation shift as a measure of donor-acceptor interaction is especially treacherous with nuclei other than protons, because chemical shifts of these nuclei are more dependent on the paramagnetic than on the diamagnetic term of the screening tensor (52, 53). Both 19F and 11B resonances of the boron trihalides do shift to high field on complexation, as expected if the complexation shift were due to the increase in electron density on the boron trihalide, and early work indicated that 19F complexation shifts of BF3 could be correlated with enthalpies of formation of the complexes. Although this is true for BF3 adducts of some series of closely related donors (42, 91, 151), such correlations do not occur in other series (169). Table II illustrates that, although there is a tendency for the strongest... [Pg.169]

A remarkable compound, comprising divalent and tetravalent tin atoms within one molecule, is the already mentioned triorganylstannylstannylene 27 the observed Sn(II)—Sn(IV) bond distance of 286.9 pm is much longer than the Sn(IV)—Sn(IV) bonds in distannanes responsible are the larger covalent radius of Sn(II) compared with Sn(rV) and the extremely bnlky Btp gronp present. It shonid be noted that a closely related donor-stabihzed stannylene is known which exhibits the same featnre,... [Pg.155]

Fig. 11. a Example of a positively solvatokinetic ground state isomerization reaction (the activation barrier decreases with increasing solvent polarity) for an aza-dervative of a donor-acceptor stilbene [94], As outlined above, related donor-acceptor-stilbenes exhibit negative solvatokinetic behavior for the excited-state reaction, b For the merocyanine dye shown, the ground state trans-cis-isomerization across the central bond shows negative solvatokinetic behavior [95], the expectation for the excited slate reaction is positive solvatokinetic behavior... [Pg.274]

Some approaches toward the synthesis and chemical modification of TTF and related donors will be mentioned only very briefly and the reader is recommended to consult more specialized reviews [213]. A common method of TTF synthesis by formation of the central exocyclic double bond starts with 1,3-dithiol-2-thione precursors 150, which are subjected to trialkyl-phosphite-induced coupling (scheme 36a) [214]. Mixed coupling products of the general... [Pg.66]

Crompton JA, Somerville T, Smith L, Corbett J, Nelson E, Holman J, Shihab FS. Lack of economic benefit with basiliximab induction in hving related donor adult renal transplant recipients. Pharmacotherapy 2003 23(4) 443-50. [Pg.418]

Cavdar C, Sifil A, Sanli E, Gulay H, Camsari T. Hypomagnesemia and mild rhabdomyolysis in living related donor renal transplant recipient treated with cyclosporine A. Scand J Urol Nephrol 1998 32(6) 415-17. [Pg.764]

Glycosylation with Glycosyl Carbonates and Related Donors. 551... [Pg.525]


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