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Synthesis of diphenyl cucurbit[6]uril (CB[6]) has been achieved via co-oligomerization of diphenyl glycoluril and unsubstituted glycoluril. The unsymmetrically substituted CB[6], Ph(2)CB[6], was further converted to a rotaxane incorporating bis(dinitrophenyl)spermine. [reaction: see text] 相似文献
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[reaction: see text] Substituted cyclopentadienone acetals (CPDAs) were synthesized by a thermal or palladium-catalyzed [3 + 2] cycloaddition reaction of a substituted cyclopropenone acetal to an electron-deficient acetylene. The synthesis afforded di-, tri-, and tetra-substituted CPDAs of considerable structural varieties that undergo Diels-Alder reaction to produce bicyclo[2.2.1]heptenes. 相似文献
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M Mitsukuchi J Nakagami T Ikemoto S Higuchi Y Tarumoto H Yasui K Sota 《Chemical & pharmaceutical bulletin》1989,37(6):1534-1539
A series of 17-succinyl derivatives of four corticosteroids was prepared. They were tested for vasoconstrictive activity in humans, using 9 alpha-fluoro-11 beta, 21-dihydroxy-16 beta-methyl-17 alpha-valeryloxy-1,4-pregnadiene-3,20-dione (betamethasone 17-valerate, BV) as a standard. The activities of the 21-chloro 17-methylsuccinate compounds (6A, 6C and 6D) were greater than that of BV. A structure-activity relationship study showed that the activities of the 21-chloro 17-methylsuccinates were more potent than those of the corresponding 21-esters. 相似文献
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Taichiro Kugo Tetsuji Kuramoto Shozo Uehara 《Zeitschrift fur Physik C Particles and Fields》1983,19(3):241-250
It is investigated to what extent the well-known algebra \(\left\{ {Q^S ,\bar Q^S } \right\} = \gamma ^\mu P_\mu \) in the rigid supersymmetry theory holds in quantum supergravity: The anti-commutator \(\left\{ {Q_\alpha ^S ,\bar Q_\beta ^S } \right\} = \gamma ^m \tilde P_m \) defines an “internal” translation generator \(\tilde P_m \) , quite another from the “external” translation generatorP μ. It is, however, shown that those two operators give the same matrix elements between any two physical states aside from a proportional factor. Such a “miracle” is caused by some particular properties of global gauge transformation charge universal in gauge theories. These properties are fully clarified in a general manner. 相似文献
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Dr. Qing‐Fu Sun Dr. Sota Sato Prof. Dr. Makoto Fujita 《Angewandte Chemie (International ed. in English)》2014,53(49):13510-13513
In the self‐assembly of PdII ions and two different, but similarly shaped, ligands ( 1 and 2 ), neither random mixing nor self‐sorting of the two ligands into two unmixed structures was observed. Instead a mixed, yet sorted, Pd12( 1 )12( 2 )12 cantellated tetrahedron (and its pseudoisomer) was selectively formed, thus revealing a fine example of intramolecular self‐sorting. A case study showed that a homothetic ratio of >2 is necessary to observe cantellated tetrahedra. 相似文献
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Taisuke Matsuno Yusuke Nakai Yutaka Maniwa Maki Someya Sota Sato Hiroyuki Isobe 《化学:亚洲杂志》2020,15(2):273-278
In a tight host–guest complex assembled solely by nondirectional van der Waals forces, unique motions of the guest, such as solid‐state inertial rotations, emerge. The regulation of dynamic motions is an important element to be explored for novel functions of such complexes, which may be seemingly difficult to achieve because of the nondirectionality of the assembling forces. A regulated, single‐axis rotation was made possible by choosing an appropriate shape of the guest in the tubular host. Specifically, an ellipsoidal guest was made to stand along a cylinder axis of the host, which consequently resulted in single‐axis rotations of the guest in the solid. The rotational frequency was considerably high for solid‐state rotations but was suppressed to 10 GHz, which was 1/20 of the isotropic rotation of a spherical guest. In‐depth kinetic analyses quantitatively revealed that the entropy cost was a determining factor that regulated the dynamics. 相似文献
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Zhe Sun Parantap Sarkar Takuya Suenaga Sota Sato Hiroyuki Isobe 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(43):12991-12995
The recent development of cyclo‐para‐phenylenes has demonstrated the feasibility of radial π systems in nanohoop structures, especially in the crystalline state. However, in contrast to macrocyclic molecules with benzene units, which have a several‐decades‐long history, macrocycles composed solely of naphthylene units (the smallest acene) have been much less explored. Although two examples of cyclonaphthylenes have been reported to date, neither possesses a radial π system. We herein report the first example of belt‐shaped cyclonaphthylenes with curved π systems. The molecule, [8]cyclo‐amphi‐naphthylene, is linked at the 2,6‐positions of the naphthylene units, thus affording belt‐shaped molecules. Although the molecular structures are flexible, which allows for rotation of the naphthylene units in solution, they can be rigidified with the aid of methylene bridges to afford persistent molecular structures in solution. 相似文献