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211.
212.
An expedient synthetic route to E-ring extended estrone derivatives is reported. Estrone-derived cyclopentenones were accessed by an intermolecular Pauson-Khand (PK) cycloaddition. It was found that electron donating and withdrawing substituents in the arylalkyne increased and decreased the yields of PK products, respectively. The stereochemistry of the products was elucidated by X-ray and NMR studies. 相似文献
213.
Jaakko Paasi Jorma Lehtonen Markku Lahtinen Lauri Kettunen 《Physica C: Superconductivity and its Applications》1998,310(1-4):62-66
A formulation for the computation of AC losses in technical HTS conductors by using commercial FEM packages developed for two-dimensional computation of electromagnetic problems is presented. The formulation takes into account the real current density–electric field characteristic of a conductor and the spatial dependence of the current density. Having presented the formulation, example runs comparing transport current loss behaviour between HTS and LTS conductors are given. 相似文献
214.
Asthana D Kumar A Pathak A Sukul PK Malik S Chatterjee R Patnaik S Rissanen K Mukhopadhyay P 《Chemical communications (Cambridge, England)》2011,47(31):8928-8930
Confluence of a modular design approach and self-assembly with a 'steroid-D-π-A' module generates spontaneous polarization in solids and for the first time in nano-architectures constituted from organogels, at room temperature (RT). 相似文献
215.
Raatikainen K Huuskonen J Rissanen K 《Dalton transactions (Cambridge, England : 2003)》2011,40(21):5706-5710
New tripodal transition metal ion receptors, tris(5-ethoxycarbonyl-2,2'-bipyridine) and tris(5-carboxylate-2,2'-bipyridine) substituted 27-membered trimeric piperazine cyclophanes 5 and 7 as well as tetra(5-ethoxycarbonyl-2,2'-bipyridine) substituted 36-membered tetrameric piperazine cyclophane 6, have been prepared and their transition metal ion complexing properties studied in solution by UV-vis spectroscopy and in the solid state by single-crystal X-ray diffraction. The crystal structures of [H(3)5(3+)·Fe(2+)]·4(ClO(4)(-))·CF(3)COO(-) (V), [H(3)7(2+)·Fe(2+)]·2(SO(4)(2-)) (VII) and the reference complex [tris(5,5'-bis(ethoxycarbonyl)-2,2'-bipyridine)Fe(II) perchlorate] (I) showed that the robust piperazine cyclophane is an optimal platform in preorganizing the 2,2'-bipy moieties to form a very fixed octahedral coordination site. In an acidic water solution, the highly preorganized structure of 5 gives a [5·Fe(2+)] complex, the stability of which is comparable with the classical tris(2,2'-bipy) Fe(2+)-complex but it is a significant 3.7 logK units more stable than the non-preorganized tetrameric analog [6·Fe(2+)]. Detailed studies with other similar divalent octahedral transition metal cations showed that the restricted octahedral coordination in complexes of 5 results in an unusual selectivity. The selectivity order [Zn(2+)相似文献
216.
Stefankiewicz AR Harrowfield J Madalan A Rissanen K Sobolev AN Lehn JM 《Dalton transactions (Cambridge, England : 2003)》2011,40(45):12320-12332
An unsymmetrical bis(tridentate) ligand LH in which one binding site can be readily deprotonated forms a kinetically inert [Co(III)L(2)](+) complex which can be used as a "corner" species for the "Coupe du Roi" assembly of trans,trans-[Co(2)M(2)L(4)](6+) metallogrids (M = Fe(II), Co(II), Cu(II), Zn(II)). In the mixed Co(III)/Co(II) species, the oxidation states appear to be localised. In solution, the ligand LH forms octacationic, homometallic [2 × 2] grids with the individual labile metal ions Fe(II), Co(II), Cu(II), Zn(II), seemingly as mixtures of all possible isomers arising from the unsymmetrical nature of the ligand. In the solid state, however, [Zn(4)L(4)](CF(3)SO(3))(8)·4CH(3)CN crystallises as a single species where the cation has S(4) symmetry. This stereoselectivity in the crystalline lattice is associated with interactions between the cation and triflate anions which can again be analysed in terms of the Coupe du Roi concept. 相似文献
217.
The synthesis and characterization of several self-assembled [4]pseudorotaxanes is reported, some of which form in a programmed way based on two similar yet orthogonal crown ether/secondary ammonium ion binding motifs. A preference for the formation of a [4]pseudorotaxane with an antiparallel rather than parallel alignment of crown ether building blocks is observed even in the absence of such orthogonal binding sites, when a homodivalent axle is used. 相似文献
218.
The JYFLTRAP double Penning trap setup at the University of Jyväskylä, Finland has been used to perform a wide range of studies related to neutron-rich fission fragments that can be produced with the Ion Guide Isotope Separator On-Line (IGISOL) method. Experimental results from high-precision mass measurements and decay-spectroscopy measurements have allowed us to investigate the nuclear structure of exotic neutron-rich nuclei. 相似文献
219.
Collin JP Durot S Keller M Sauvage JP Trolez Y Cetina M Rissanen K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(3):947-957
A new example of a linear [5]rotaxane has been synthesized by using the traditional "gathering-and-threading" approach but based on an unusual axle incorporating a symmetrical bis(bidentate) chelating fragment built on a 4,7-phenanthroline core. The stoppering reaction is particularly noteworthy since, instead of using a trivial bulky stopper as precursor to the blocking group, two semistoppered copper-complexed [2]pseudorotaxanes (namely [2]semirotaxanes) are used, which leads to the desired [5]rotaxane in good yield. The efficiency of the method relies on the use of "click" chemistry, with its very mild conditions, and on the protection by a transition-metal (copper(I)) of the various coordinating groups present in the fragments to be interconnected (terpy and bidentate chelating groups), thus inhibiting potential detrimental side reactions during the copper-catalyzed stoppering reaction. Since the external fragments and the central core of the system contain tri- and bidentate chelating units, respectively, the axle of the final [5]rotaxane incorporates two types of coordinating units: two external terpy groups (terpy: 2,2':6',2'-terpyridine) and two central bidentate ligands. Such a situation enables the system to tidy two different metals centers, and to localize them in a priori well-defined positions. This is what was observed when mixing the free ligand with a mixture of Zn(2+) and Li(+) : the zinc(II) ions were unambiguously shown to occupy the external sites, whereas the Li(+) cations were found in the central part of the [5]rotaxane. An X-ray diffraction study carried out on a [3]pseudorotaxane, the axis of which is similar to the central part of the [5]rotaxane axle, demonstrates that Zn(2+) is clearly five-coordinate, the fifth ligand being a counterion, even when the coordination site of the pseudorotaxane is designed for four-coordinate metals, which is in marked contrast with copper(I) or Li(+) . 相似文献
220.
Iko Hyppänen Jorma Hölsä Jouko Kankare Mika Lastusaari Laura Pihlgren Tero Soukka 《Journal of fluorescence》2011,21(3):963-969
Up-converting NaRF4-NaR′F4 (R: Y, Yb, Er) nanomaterials with different core-shell combinations were prepared with the co-precipitation method. The X-ray
powder diffraction (XPD) measurements revealed the presence of both the cubic and hexagonal NaRF4 phases. The crystallite sizes calculated with the Scherrer formula were 100 and 150 nm for the cubic and hexagonal phases,
respectively. The FT-IR spectra showed water impurities. The up-conversion luminescence and luminescence decays were studied
with NIR laser excitation at 970 nm. The up-conversion luminescence spectra showed strong red (640–685 nm) (4F9/2 → 4I15/2) and moderate green (515–560 nm) (2H11/2,
4S3/2 → 4I15/2) Er3+ luminescence. The strongest up-conversion luminescence and longest red luminescence decay was obtained from the Na(Y,Yb)F4-NaErF4 core-shell combination. 相似文献