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Douglas S. Shephard Wuzong Zhou Thomas Maschmeyer Justin M. Matters Caroline L. Roper Simon Parsons Brian F. G. Johnson Melinda J. Duer 《Angewandte Chemie (International ed. in English)》1998,37(19):2719-2723
The “staining” cluster–crown compound [Ru6C(CO)14(η6-C6H4C10H20O6)] verifies that the internal walls of mesoporous silica MCM-41 may be selectively functionalized with propylammonium groups (see picture). By the use of high-resolution transmission electron microscopy the presence and position of the cluster and also of the functional groups may be directly determined. 相似文献
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Reactions of the dichloroboryl complex of osmium, Os(BCl2)Cl(CO)(PPh3)2, with water, alcohols, and amines: Crystal structures of Os[B(OH)2]Cl(CO)(PPh3)2, Os[B(OEt)2]Cl(CO)(PPh3)2, and
George R. Clark Geoffrey J. Irvine Warren R. Roper L. James Wright 《Journal of organometallic chemistry》2003,680(1-2):81
Reaction between the dichloroboryl complex, Os(BCl2)Cl(CO)(PPh3)2, and water replaces both chloride substituents on the boryl ligand, without cleavage of the Os---B bond, giving yellow Os[B(OH)2]Cl(CO)(PPh3)2 (1). Compound 1 can be regarded as an example of a ‘metalla–boronic acid’ (LnM---B(OH)2) and in the solid state, X-ray crystal structure determination reveals that molecules of 1 are tetragonal pyramidal in geometry (Os---B, 2.056(3) Å) and are arranged in pairs, as hydrogen-bonded dimers. This same arrangement is found in the crystalline state for simple boronic acids. Reaction between the dichloroboryl complex, Os(BCl2)Cl(CO)(PPh3)2, and methanol and ethanol produces yellow Os[B(OMe)2]Cl(CO)(PPh3)2 (2a) and yellow Os[B(OEt)2]Cl(CO)(PPh3)2 (2b), respectively. The crystal structure of 2b reveals a tetragonal pyramidal geometry with the diethoxyboryl ligand in the apical site and with an Os---B bond distance of 2.081(5) Å. Reaction between Os(BCl2)Cl(CO)(PPh3)2, and N,N′-dimethyl-o-phenylenediamine and N,N′-dimethyl-ethylenediamine produces yellow
(5) and yellow
(6), respectively. Compounds 1, 2a, 2b, 5, and 6 all react with carbon monoxide to give the colourless, six-coordinate complexes Os[B(OH)2]Cl(CO)2(PPh3)2 (3), Os[B(OMe)2]Cl(CO)2(PPh3)2 (4a), Os[B(OEt)2]Cl(CO)2(PPh3)2 (4b),
(7), and
(8), respectively, but in the case of 6 only, this CO uptake is easily reversible. The crystal structure of 5 is also reported. 相似文献
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Caddell JM Chapman AM Cooley BE Downey BP LeBlanc MP Jackson MM O'Connell TM Phung HM Roper TD Xie S 《The Journal of organic chemistry》2004,69(9):3212-3215
A convergent synthesis of adenosine A2a agonist 1 in the form of its maleate salt 2 was achieved. The key step in this approach was the highly selective 9beta-glycosylation reaction between 2-haloadenines or an N(2)-alkyl-6-chloroguanine and a D-ribose derivative containing a 2-ethyltetrazolyl moiety. Glycosylations of other purine derivatives were also examined, and the methods developed provide efficient access to a variety of adenosine analogues such as 2-alkylaminoadenosines, an attractive class of compounds with antiinflammatory activity. 相似文献
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N. Allen N. H. Furman E. Krause R. Becker P. Pfeiffer K. Schnurmann R. F. Chambers Ph. C. Scherer W. F. Hillebrand G. E. F. Lundell D. S. Reynolds W. H. Roß K. D. Jacob O. B. Winter Lillian Butler F. J. Frere G. Batchelder V. W. Meloche I. Tananaeff H. Flisik E. C. Roper E. B. R. Prideaux P. Drawe W. Rehwinkel L. Dupare P. Wenger und G. Graz 《Fresenius' Journal of Analytical Chemistry》1934,96(5-6):211-223
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