First, some general remarks concerning macroscopic “cluster matter” are given. In the second part, three recent, mainly optically and electron-microscopically performed investigations are discussed which deal with special properties of noble metal cluster systems forming the building units of this kind of matter:(1) dressed Au-55 clusters,(2) electromagnetic coupling effects among coagulated clusters,(3) the transition towards compact inhomogeneous matter caused by coalescence of clusters. 相似文献
The intramolecular Friedel-Crafts cyclisation of ω-arylalkanoic acids, which is in the benzene series a valuable synthetic route to bicyclic ketones with medium-sized and large rings, has been investigated with ω-(1-naphthyl)alkanoyl chlorides. The lower members, including naphthyl-caproic acid, close the ring at position 2 to form IV. The higher homologous acids show a preference for annellation at 7, making available a new type of heteronuclear naphthalene cyclic ketones (VII). During cyclisation of ω-(1-naphthyl) decanoic acid, the 1,4 ring closure competes with the 1,7 type.
Steric hindrance of resonance as a consequence of “medium ring torsion” was studied in different classes of naphthocyclenones. 相似文献
The crystal and molecular structures of two quarternary salts of 2-oxosparteine (II), the methiodide (IICH+3 • I−) and the methperchlorate (IICH+3 • ClO−4) have been determined on the basis of X-ray and IR data. The studies were performed by analogy to previously investigated quaternary salts of sparteine (I), the methiodide (ICH+3 • I−) and the methperchlorate (ICH+3 • ClO−4). As expected, the configurations and conformations of cationic parts within the two pairs of quaternary salts are identical, except for the structure of their A/B fragments, which in ICH+3 cations have the character of tertiary amines, but in IICH+3 that of lactams.
On the basis of accumulated X-ray and IR data the similarities and differences in the modes of interaction of perchlorate and iodide anions with quaternary cations, and especially with their N+---CH3 groups are discussed. In this discussion are also included the methiodide and methperchlorate of -isosparteine: IIICH+3 • X− (X− = I− or ClO−4) where N+---CH3 groups are cisoidally oriented to the basic nitrogen atoms. The most interesting observations are as follows: (i) When N+---CH3 groups are easily accessible for direct quasi hydrogen bonding interactions with counter anions and when other positive charged groups, for instance lactam groups, are absent in quaternary cations, perchlorate anions interact more strongly than the iodide anions and in consequence introduce conformational changes into the ring with N+---CH3 group as well as into further rings. (ii) Perchlorate and iodide anions interact with N+---CH3 groups similarly and very weakly if at all, when the N+---CH3 groups are for steric reasons inaccessible to counter anions or when in quaternary cations there are additional groups which attract the counter anions electrostatically. The last mechanism operates in both quaternary salts of 2-oxosparteine and this is the reason why their monocrystals are isosteric and IR spectra almost identical. (iii) The sterically hindered N+---CD3 groups in both IIICD+3 • X− salts give rise in their IR spectra to two doubles of sharp, well resolved bands which indicate the presence of two different rotamers stabilized by two modes of weak intramolecular hydrogen bonds with basic N atoms. (iv) In IIICH+3 • X− and IIICD+3 • X− salts the perchlorate and iodide anions do not interact at all with the rotating and vibrating N+---CH3 (N+---CD3) group but the structures of these salts are not isosteric since the perchlorate anions interact more strongly than iodide anions with the A/B fragment of the IIICH+3 cations. This is visible from the shapes and intensities of the so-called “trans” band in the IR spectra of both salts. 相似文献
The results of transient loss measurements performed in a self-sustained discharge KrF* amplifier are reported. Analysis of these results gives a minimum value of 20 for the effective gain to loss ratiog0/eff, indicating that efficient extraction of energy in subpicosecond KrF* amplifiers in the 1 J range should be achievable. 相似文献
The critical exponents , and of undeuterated and partially deuterated ferroelectric betaine arsenate are estimated. Small but remarkable deviations from the tricritical values are observed. The obtained values are tested via scaling of the isothermals.At some distance aboveTc a cross-over of the effective critical exponent to a value typically for short-range forces is observed. A suitably defined cross-over temperature range decreases with increasing deuteration and seems to vanish near the antiferroelectric phase boundary. 相似文献
In the tree approximation, the critical relaxational dynamics of 2n with quenched random fields is calculated by renormalization near the upper critical dimensiondu=4+2/(n–1). Although the relation between the characteristic frequency cq and the wave-numberq is as usual,unusual results are obtained for the asymptotic decay of the order-parameter correlation functionS(q,t).Dedicated to Prof. Dr. W. Döring on the occasion of his 75th birthday 相似文献
The hexagonal Jahn-Teller compounds ABCl3 (A=Cs, Rb; B=Cu, Cr) in their common high temperature phase are modeled as a system of independent elastic dipoles dressed by a far reaching strain field. The diffuse elastic cross section for neutrons is derived as for Huang scattering. Isointensity contours and line widths (FWHM) are calculated for CsCuCl3 and compared to experimental results, especially looking for correlations and precursor effects of the structural phase transition. 相似文献
Summary Real hypersurfaces of an almost Hermitian manifold naturally admit an almost contact metric structure and the (f, g, u, v, w, , , )-structure is defined on submanifolds of codimension 3 of an almost Hermitian manifold. We study the so-called semi-invariant submanifolds of a complex space form with almost contact metric compound structure which is a general notion of (f, g, u, v, w, , , )-structure.Dedicated to professor Eulyong Pak on his 60th birthdayThis research was partially supported by Korean Science and Engineering Foundation Grant. 相似文献