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101.
[reaction: see text] Regio- and stereoselective deprotonation of N-Bus (Bus = tert-butylsulfonyl)-protected terminal aziridines with lithium 2,2,6,6-tetramethylpiperidide generates a nonstabilized (H-substituted) aziridinyl anion that undergoes in situ or external electrophile trapping under experimentally straightforward conditions to give trans-disubstituted aziridines in good to excellent yields. 相似文献
102.
Arnold P Ward J Wilson D Ashley Guthrie J Robinson PJ 《Magnetic resonance imaging》2003,21(7):695-700
The aim of this study was to establish whether enhancement of the liver by the MRI contrast agent ferumoxides could be effectively achieved at a reduced dose of 7.5 micromol/kg in patients with advanced liver cirrhosis. Forty-two liver transplant candidates with end-stage cirrhosis underwent SPIO-enhanced MRI at 1.5T, using either 15 micromol/kg or 7.5 micromol/kg ferumoxides. The lower dose of ferumoxides was also used in 21 non-cirrhotic patients with colorectal liver metastases who acted as a control group. The percentage signal intensity loss (PSIL) after SPIO was measured in all patients, and in those patients with tumors the post-SPIO contrast-to-noise ratio (CNR) was measured. The median PSIL after SPIO in the high dose cirrhotic (HDLC), low dose non-cirrhotic (LDNC) and low dose cirrhotic (LDLC) patients was 86.3%, 74.6%, and 64.2% respectively. These differences were significant using the Mann-Whitney U test. Tumors were found in 8 patients in the high dose cirrhotic group, 9 in the low dose cirrhotic group, and all 21 of the control group. No significant differences were found between the CNR values after SPIO in the 3 groups (median values HDLC 15.1, LDNC 23.7, LDLC 19.5). In patients with late-stage cirrhosis the PSIL after SPIO was significantly less at 7.5 micromol/kg than at 15 micromol/kg, but both doses produced a substantial loss of signal. Lesion to liver CNR was not adversely affected by using the lower dose, so when imaging at 1.5T the authors would recommend using 7.5 micromol/kg in patients with liver cirrhosis. 相似文献
103.
Shavaleev NM Moorcraft LP Pope SJ Bell ZR Faulkner S Ward MD 《Chemical communications (Cambridge, England)》2003,(10):1134-1135
In a series of heterodinuclear complexes in which a Pt(PPh3)2(catecholate) chromophore is covalently linked to a lanthanide tris(diketonate) unit, sensitised near-IR emission from Yb(III), Nd(III) and Er(III) occurs on excitation of the Pt(II) chromophore at 520 nm. 相似文献
104.
Gamblin DP Garnier P Ward SJ Oldham NJ Fairbanks AJ Davis BG 《Organic & biomolecular chemistry》2003,1(21):3642-3644
Controlled site-selective glycosylation can be achieved by combining site-directed cysteine mutagenesis with chemical modification of the introduced thiol; a new class of more efficient chemoselective reagents, glycosyl phenylthiosulfonates, allow rapid glycosylations of representative simple thiols, peptides and proteins. 相似文献
105.
Plaut DJ Martin SM Kjaer K Weygand MJ Lahav M Leiserowitz L Weissbuch I Ward MD 《Journal of the American Chemical Society》2003,125(51):15922-15934
Crystalline ternary inclusion monolayers consisting of a two-dimensional hydrogen-bonded host network of guanidinium (G) ions and organosulfonate (S) amphiphiles, and biphenylalkane guests, can be generated at the air-water interface through synergistic structural enforcement by hydrogen bonding and host-guest packing. Surface pressure-area isotherms of the 4'-hexadecylbiphenyl-4-sulfonate (C16BPS) amphiphile in the presence of G, with or without guest, are characterized by lift-off molecular areas expected for the GS sheet based on single-crystal X-ray structures of homologous bulk crystals. Intercalation of biphenylalkane guests (4-C(n)()H(2)(n)()(+1)-C(6)H(4)-C(6)H(5), n = 1, 4, 6, 10, 16; denoted CnBP) between organosulfonate hydrophobes, which define pocketlike cavities in the GS monolayer host, afford ternary inclusion monolayers with a 1:1 host-guest stoichiometry. These inclusion monolayers are less compressible than the guest-free host, consistent with dense packing of the biphenylalkane moieties of the host and the biphenylalkane guests. The inclusion monolayers are distinguished from the amorphous guest-free host and from selected guanidinium-free mixed monolayers by structural characterization with grazing-angle incidence X-ray diffraction (GIXD). The GIXD data for the ternary (G)C16BPS:C16BP and (G)C16BPS:C6BP inclusion monolayers obtained upon compression are consistent with a rectangular unit cell. The dimensions of these unit cells and refinement of the GIXD data suggest a "rotated shifted ribbon" GS hydrogen-bonding motif similar to that observed in some bulk GS crystals, including (G)(ethylbiphenylsulfonate). GIXD reveals that (G)C16BPS:C16BP and (G)C16BPS:C6BP are more crystalline than the corresponding guanidinium-free mixed monolayers. The (G)C16BPS:C6BP inclusion monolayer is stable upon compression, even though the alkyl-alkyl host-guest interactions are reduced due to the shorter hexyl substituents of the guest, demonstrating an important reinforcing role for the hydrogen-bonded GS sheet. The structure of a C16BPS:tetracosane (C24) mixed monolayer is independent of G; the unit cell symmetry and dimensions suggest a structure governed by alkyl-alkane interactions that prohibit formation of a GS network. These results illustrate that the existence of ternary inclusion monolayers with an intact GS network requires guest molecules that are structurally homologous with the hydrophobes of the host, in this case biphenylalkanes. The observation of these inclusion compounds suggests an approach for introducing functional nonamphiphilic molecules to an air-water interface through inclusion in a well-defined host. 相似文献
106.
107.
N. S. Kelsall C. E. Svensson S. Fischer D. E. Appelbe R. A. E. Austin D. P. Balamuth G. C. Ball J. A. Cameron M. P. Carpenter R. M. Clark M. Cromaz M. A. Deleplanque R. M. Diamond P. Fallon D. F. Hodgson R. V. F. Janssens D. G. Jenkins G. J. Lane C. J. Lister A. O. Macchiavelli C. D. O’Leary D. G. Sarantities F. S. Stephens D. C. Schmidt D. Seweryniak K. Vetter J. C. Waddington R. Wadsworth D. Ward A. N. Wilson A. V. Afanasjev S. Frauendorf I. Ragnarsson 《The European Physical Journal A - Hadrons and Nuclei》2003,20(1):131-132
High-spin states have been studied in 72Kr and 72Br using the 40Ca + 40Ca and 36Ar + 40Ca reactions at 164 and 145 MeV, respectively. The properties and configurations of the high-spin bands observed have been interpreted using unpaired cranked Nilsson-Strutinsky (CNS), and for 72Kr, paired cranked relativistic Hartree-Bogoliubov (CRHB) calculations. In 72Kr a new band has been identified that has the properties expected for the doubly aligned S-band configuration. In 72Br the previously known bands have been extended to higher spin. This has lead to a re-interpretation of the configurations.Received: 31 October 2002, Published online: 24 February 2004PACS:
21.10.Re Collective levels - 23.20.Lv
transitions and level energies - 27.50. + e
相似文献
108.
Studies of the behaviour with 1, 2 and film thickness of the optical functions reflectance (R) and phase change on reflection (Φr) have previously been made for both very thin and very thick films. Abelès [J. Opt. Soc. Amer. 47 (1957) 473] has formulated equations for very thin films where functions of 1 and 2 are the coefficients of a power series of the optical thickness, x(2πd/λ) up to x2, whilst in the case of very thick films (solids) the relationships between 1 and 2 can be represented in polar coordinates L and α by 1=L cos α, 2=L sin α where LR=2y20W2(1+cos α−1/W2) [W=(1+R)/(1−R)] and LΦr=2(y0/ tan Φr)2(1−cos α+tan 2 Φr) [Ward, Opt. and Laser Tech. 27 (1995) 125]. The present study is concerned with films of intermediate optical thicknesses (1.0<2πd/λ<solid) and has revealed that the polar-type relationships previously noted for solid materials are augmented by secondary structures of maxima and minima whose position and amplitude can be predicted by adapting the exact equations for R and Φr. 相似文献
109.
110.
MtsslWizard is a computer program, which operates as a plugin for the PyMOL molecular graphics system. MtsslWizard estimates
distances between spin labels on proteins quickly with user-configurable options through a simple graphical interface. In
default mode, the program searches for ensembles of possible MTSSL conformations that do not clash with a static model of
the protein. Once conformations are assigned, distance distributions between two or more ensembles are calculated, displayed,
and can be exported to other software. The program’s use is evaluated in a number of challenging test cases and its strengths
and weaknesses evaluated. The benefits of the program are its accuracy and simplicity. 相似文献