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81.
Laurent P Miyaji H Collinson SR Prokes I Moody CJ Tucker JH Slawin AM 《Organic letters》2002,4(23):4037-4040
A new strategy for the asymmetric synthesis of chiral primary alpha-ferrocenylalkylamines has been utilized to generate homochiral redox-active receptors that bind chiral carboxylate anions with moderate enantioselectivity and undergo a redox response to complexation. [structure: see text] 相似文献
82.
Anzenbacher P Jursíková K Shriver JA Miyaji H Lynch VM Sessler JL Gale PA 《The Journal of organic chemistry》2000,65(22):7641-7645
Lithiation and subsequent addition of an electrophile to meso-octamethylcalix[4]pyrrole provides a straightforward synthetic route to new, C-rim monosubstituted calix[4]pyrroles. A variety of electrophiles were used, resulting in calix[4]pyrroles with appended functional groups including carboxyl, ester, iodo, and formyl. This method was optimized to give maximum yields of the monosubstituted derivatives with lowest possible contamination by di- and trisubstituted congeners. Solid-state studies, performed for a number of these derivatives, showed unexpected supramolecular interactions involving both solvents and the monosubstituted calix[4]pyrrole derivatives themselves. 相似文献
83.
84.
A Complex Perovskite‐Type Oxynitride: The First Photocatalyst for Water Splitting Operable at up to 600 nm
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Dr. Chengsi Pan Dr. Tsuyoshi Takata Mamiko Nakabayashi Dr. Takao Matsumoto Prof. Naoya Shibata Prof. Yuichi Ikuhara Prof. Kazunari Domen 《Angewandte Chemie (International ed. in English)》2015,54(10):2955-2959
One of the simplest methods for splitting water into H2 and O2 with solar energy entails the use of a particulate‐type semiconductor photocatalyst. To harness solar energy efficiently, a new water‐splitting photocatalyst that is active over a wider range of the visible spectrum has been developed. In particular, a complex perovskite‐type oxynitride, LaMgxTa1?xO1+3xN2?3x (x≥1/3), can be employed for overall water splitting at wavelengths of up to 600 nm. Two effective strategies for overall water splitting were developed. The first entails the compositional fine‐tuning of a photocatalyst to adjust the bandgap energy and position by forming a series of LaMgxTa1?xO1+3xN2?3x solid solutions. The second method is based on the surface coating of the photocatalyst with a layer of amorphous oxyhydroxide to control the surface redox reactions. By combining these two strategies, the degradation of the photocatalyst and the reverse reaction could be prevented, resulting in successful overall water splitting. 相似文献
85.
Recent pump-probe experiments with intense femtosecond laser pulses and diatomic molecules N2 and O2, have revealed the presence of Raman-forbidden anomalous series and lines in the Fourier spectrum of HHG (high harmonic generation) signals. A theoretical analysis of the problem is made by deriving a general expression of the angle dependent HHG operator that governs the dynamic alignment signals in linear molecules, and applying them to the experiments in N2 and O2. A unified interpretation of the origin of the observed Raman-allowed and the anomalous spectral features is given. The results are also used to estimate the molecular temperature in the experiments. 相似文献
86.
The occurrence of a heteroatom X (C, N, or O) in the MoFe7S9X core of the iron-molybdenum cofactor of nitrogenase has encouraged synthetic attempts to prepare high-nuclearity M-Fe-S-X clusters containing such atoms. We have previously shown that reaction of the edge-bridged double cubane [(Tp)2Mo2Fe6S8(PEt3)4] (1) with nucleophiles HQ- affords the clusters [(Tp)2Mo2Fe6S8Q(QH)2](3-) (Q = S, Se) in which HQ- is a terminal ligand and Q(2-) is a mu2-bridging atom in the core. Reactions with OH- used as such or oxygen nucleophiles generated in acetonitrile from (Bu3Sn)2O or Me3SnOH and fluoride were examined. Reaction of 1 with Et4NOH in acetonitrile/water generates [(Tp)2Mo2Fe6S9(OH)2]3- (3), isolated as [(Tp)2Mo2Fe6S9(OH)(OC(=NH)Me)(H2O)](3-) and shown to have the [Mo2Fe6(mu2-S)2(mu3-S)6(mu6-S)] core topology very similar to the P(N) cluster of nitrogenase. The reaction system 1/Et4NOH in acetonitrile/methanol yields the P(N)-type cluster [(Tp)2Mo2Fe6S9(OMe)2(H2O)](3-) (5). The system 1/Me3SnOH/F- affords the oxo-bridged double P(N)-type cluster {[(Tp)2Mo2Fe6S9(mu2-O)]2}5- (7), convertible to the oxidized cluster {[(Tp)2Mo2Fe6S9(mu2-O)]2}4- (6), which is prepared independently from [(Tp)2Mo2Fe6S9F2(H2O)](3-)/(Bu3Sn)2O. In the preparations of 3-5 and 7, hydroxide liberates sulfide from 1 leading to the formation of P(N)-type clusters. Unlike reactions with HQ-, no oxygen atoms are integrated into the core structures of the products. However, the half-dimer composition [Mo2Fe6S9O] relates to the MoFe7S9 constitution of the putative native cluster with X = O. (Tp = hydrotris(pyrazolyl) borate(1-)). 相似文献
87.
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89.
Nobuhiro Kanomata Masayuki Suzuki Mamiko Yoshida Tadashi Nakata 《Angewandte Chemie (International ed. in English)》1998,37(10):1410-1412
Just like in biological systems , the GAPDH-catalyzed oxidation of aldehyde to carboxylate proceeds in conjunction with 1,4-selective reduction of NAD+ to NADH model compounds [Eq. (1)]. The combination of GAPDH- and LDH-type transfer reactions is also described here as a system mimic for the NAD+/NADH redox cycle in anaerobic glycolysis. GAPDH=D -glyceraldehyde-3-phosphate dehydrogenase, LDH=L -lactate dehydrogenase. 相似文献
90.
Inside Cover: A Complex Perovskite‐Type Oxynitride: The First Photocatalyst for Water Splitting Operable at up to 600 nm (Angew. Chem. Int. Ed. 10/2015)
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