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51.
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L. Sommer 《Fresenius' Journal of Analytical Chemistry》1966,220(3):222-223
Ohne Zusammenfassung 相似文献
53.
L. Sommer 《Fresenius' Journal of Analytical Chemistry》1966,216(3):351-352
Ohne Zusammenfassung 相似文献
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Niu W Wong EH Weisman GR Hill DC Tranchemontagne DJ Lam KC Sommer RD Zakharov LN Rheingold AL 《Dalton transactions (Cambridge, England : 2003)》2004,(21):3536-3547
Ethylene cross-bridging of the popular tetraazamacrocyclic ligand cyclam has led to metal complexes with enhanced kinetic inertness. The synthesis and spectral characterization of zinc(II), cadmium(II), and mercury(II) complexes of cross-bridged cyclam (L1) as well as cross-bridged cyclen (L2) are reported along with the details of our synthetic route to L2. X-ray structural studies revealed that all Zn(II) and Cd(II) cations are fully kappa(4)N-coordinated inside the respective ligand's molecular cleft with L1 providing the better fit for Zn(II). While Hg(II) is similarly coordinated to L2, it has been found to complex L1 outside the ligand cleft in a novel exo-kappa(2)N-mode. Solution NMR data of the kappa(4)N complexes are consistent with the presence of only a single cis-folded isomer in each case. Ligand (1)H and (13)C coupling to both (111,113)Cd and (199)Hg in their complexes can be clearly discerned. The relative kinetic inertness of representative cross-bridged complexes in acidic aqueous solution has been assessed and found to be in the following order: Zn(II) > Cd(II)[dbl greater-than] Hg(II). The data also reaffirm that cross-bridged cyclam ligand L1 forms a substantially more inert complex with zinc(II) than either the smaller cyclen analogue L2 or the unbridged 1,4,8,11-tetramethyl-cyclam L3. 相似文献
57.
Isomorphism is an equivalence relation that is less stringent than identity (equality), and it is useful for synthetic analysis, since it allows one to find reflexive routes for targets even when they do not have an element of symmetry. 相似文献
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Gerritz SW Norman MH Barger LA Berman J Bigham EC Bishop MJ Drewry DH Garrison DT Heyer D Hodson SJ Kakel JA Linn JA Marron BE Nanthakumar SS Navas FJ 《Journal of combinatorial chemistry》2003,5(2):110-117
The high-throughput manual solid-phase parallel synthesis of libraries comprising thousands of discrete samples using pellicular supports (i.e. SynPhase crowns and lanterns) and a suite of novel tools and techniques is described. Key aspects of this approach include the combination of a split-split-split synthesis strategy with spatial encoding to differentiate thousands of crowns, the rapid washing and filtration of up to 48 reaction vessels in parallel, the application of an inexpensive and environmentally friendly technique to remove trifluoroacetic acid from sixteen 96-well plates in parallel, and a high-throughput method for removing cleaved crowns from reusable pin racks. Tens of thousands of discrete samples have been produced in-house using this conceptually and operationally straightforward strategy. 相似文献
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P. Schmid K. Uran F. Macherey M. Ebert H.-J. Ullrich D. Sommer F. Friedel 《Analytical and bioanalytical chemistry》2009,393(8):1863-1870
The formation of Fe–Zn intermetallic compounds, as relevant in the commercial product galvannealed steel sheet, was investigated
by scanning electron microscopy and different methods of X-ray diffraction. A scanning electron microscope with high resolution
was applied to investigate the layers of the galvannealed coating and its topography. Grazing incidence X-ray diffraction
(GID) was preferred over conventional Bragg–Brentano geometry for analysing thin crystalline layers because of its lower incidence
angle α and its lower depth of information. Furthermore, in situ experiments at an environmental scanning electron microscope (ESEM)
with an internal heating plate and at an X-ray diffractometer equipped with a high-temperature chamber were carried out. Thus,
it was possible to investigate the phase evolution during heat treatment by X-ray diffraction and to display the growth of
the ζ crystals in the ESEM. 相似文献