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141.
The original article to which this Erratum refers was published in Magnetic Resonance in volume 45 issue 1.  相似文献   
142.
143.
An integral formula is derived, relating the six irreducible components of the intrinsic torsion of an SpnSp1 structure on a compact 4n-dimensional manifold with the Riemann curvature tensor. Some consequences of the formula are studied.  相似文献   
144.
Steaming resulted in modification of the distribution of acid strength of OH groups. The contribution of less acidic sites increased and new, very strongly acidic hydroxyls characterized by IR band at 3590 cm-1 appeared.  相似文献   
145.
PAC experiments using181Hf as probe atom were performed in Ta samples containing 1.1 at% of N and loaded with 0.2 at% of H or of 1.6 at% of D. At room temperature only the known frequency due to N is present. Below 100K or 140K, for H and D respectively, the amplitude of this interaction decreases and two new interaction frequencies characterized by V0=240MHz, η=0.80 and V0=250 MHz, η=0.40 appear. These frequencies are attributed to H(D) trapped by N in the vicinity of the probe atom181Hf. The disappearance of these interactions at 100K and 140K is interpreted as a release of H (D) from Hf but not from N. From the data the jump rates of H(D) around N in Ta are derived.  相似文献   
146.
5‐Ethynyl‐2,2′‐bipyridine ( 1 ; bpyC≡CH) polymerized in the presence of catalytic amounts of [RhF(COD)(PPh3)] or [Rh(μ‐OH)(COD)]2 (COD = 1,5‐cyclooctadiene) in 74–91% yields. In contrast, [Rh(μ‐X)(NBD)]2 (X = Cl or OMe; NBD = norbornadiene) did not catalyze the polymerization of 1 or gave low yields of the polymer. The obtained polymer, poly(5‐ethynyl‐2,2′‐bipyridine) [ 2 ; (bpyC?CH)n], was highly stereoregular with a predominant cis–transoidal geometry. Random copolyacetylenes containing the 2,2′‐bipyridyl group with improved solubility in organic solvents were obtained by the treatment of a mixture of 1 and phenylacetylene ( 3 ) or 1‐ethynyl‐4‐n‐pentyl‐benzene with catalytic amounts of [RhF(COD)(PPh3)]. A block copolymer of 1 and 3 was prepared by the addition of 1 to a poly(phenylacetylene) containing a living end. The reaction of 2 with [Mo(CO)6] produced an insoluble polymer containing [Mo(CO)4(bpy)] groups, whereas with [RuCl2(bpy)2] or [Ru(bpy)2(CH3COCH3)2](CF3SO3)2, it gave soluble metal–polymer complexes containing [Ru(bpy)3]2+ groups. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43:3167–3177, 2005  相似文献   
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148.
New asymptotic approximations of the noncentral t distribution are given a generalization of the Student's t distribution. Using new integral representations, we give new asymptotic expansions not only for large values of the noncentrality parameter but also for large values of the degrees of freedom parameter. In some cases, we accept more than one large parameter. These results are not only in terms of elementary functions, but also in terms of the complementary error function and the incomplete gamma function. A number of numerical tests demonstrate the performance of the asymptotic approximations.  相似文献   
149.
Small alterations to the structure of a star‐shaped template totally change its mode of operation. The hexapyridyl template directs the conversion of a porphyrin dimer to the cyclic hexamer, but deleting one pyridine site changes the product to the cyclic decamer, while deleting two binding sites changes the product to the cyclic octamer. This surprising switch in selectivity is explained by the formation of 2:1 caterpillar track complexes, in which two template wheels bind inside the nanoring. Caterpillar track complexes can also be prepared by binding the hexapyridyl template inside the 8‐ and 10‐porphyrin nanorings. NMR exchange spectroscopy (EXSY) experiments show that these complexes exhibit correlated motion, in which the conrotatory rotation of the two template wheels is coupled to rotation of the nanoring track. In the case of the 10‐porphyrin system, the correlated motion can be locked by binding palladium(II) dichloride between the two templates.  相似文献   
150.
In this work, the new polyamine bisnaphthalimidopropyl‐4,4’‐diaminodiphenylmethane is proposed as a new ionophore for perchlorate potentiometric sensors. The optimal formulation for the membrane comprised of 12 mmol kg?1 of the ionophore, and 68 % (w/w) of 2‐nitrophenyl phenyl ether as plasticizer and 31 % (w/w) of high molecular weight PVC. The sensors were soaked in water for a week to allow leakage of anionic impurities and for one day in a perchlorate solution (10?4 mol L?1) to improve reproducibility due to its first usage. The stability constant for the ionophore‐perchlorate association in the membrane, log βIL1=3.18±0.04, ensured a performance characterized by the slope of 54.1 (±0.7) mV dec?1 to perchlorate solutions with concentrations between 1.24×10?7 and 1.00×10?3 mol L?1. The sensors are insensitive to pH between 3.5 to 11.0, they have a practical detection limit of 7.66 (±0.42) ×10?8 mol L?1 and a response time below 60 s for solutions with perchlorate concentrations above 5×10?6 mol L?1. The accuracy of the results was confirmed by the analysis of the contaminant in a certified reference water sample.  相似文献   
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