Design and Evaluation of Computer Generated Hologram with Binary Subwavelength Structure Designed by Deterministic Process

A binary subwavelength structure for multilevel phase modulation can be designed by our previously proposed deterministic design method without iterative optimization method. To use our design technique in various applications of a computer generated hologram (CGH) like an array illuminator, beam-shaping, signal processing, and so on, an image quality of a reconstructed image from a CGH has become much more important. In this paper, we verify the image quality of a reconstructed image from a CGH designed by our method in terms of the modulation transfer function (MTF) and the spatial resolution. Simulation results show that our technique can theoretically achieve a MTF of more than 99% over a wide range and a spatial resolution of less than 9.66μm.     

A Triphenylamine with Two Phenoxy Radicals Having Unusual Bonding Patterns and a Closed‐Shell Electronic State

Reported herein is the structure and the electronic properties of a novel triphenylamine derivative having two phenoxy radicals appended to the amino nitrogen atom. X‐ray single crystal analysis and the magnetic resonance measurements demonstrates the unexpected closed‐shell electronic structure, even at room temperature, of the molecule and two unusual C? N bonds with multiple‐bond character. The theoretical calculations support the experimentally determined molecular geometry with the closed‐shell electronic structure, and predicted a small HOMO–LUMO gap originating from the nonbonding character of the HOMO. The optical and electrochemical measurements show that the molecule has a remarkably small HOMO–LUMO gap compared with its triphenylamine precursor.     

Microbial conversion of curcumin into colorless hydroderivatives by the endophytic fungus Diaporthe sp. associated with Curcuma longa

We investigated the microbial conversion of curcumin (1) using endophytic fungi associated with the rhizome of Curcuma longa (Zingiberaceae). We found that Diaporthe sp., an endophytic filamentous fungus, converts curcumin (1) into four colorless derivatives, namely (3R,5R)-tetrahydrocurcumin (2), a novel (3R,5S)-hexahydrocurcumin (3) named neohexahydrocurcumin, (3S,5S)-octahydrocurcumin (4) and meso-octahydrocurcumin (5).     

Spicachlorantins G-J, new lindenane sesquiterpenoid dimers from the roots of Chloranthus spicatus

Four new lindenane sesquiterpenoid dimers, spicachlorantins G-J (1-4), were isolated from the roots of Chloranthus spicatus together with seven known compounds, including chloramultilide A, shizukaol B, shizukaol D, shizukaol F, shizukaol P, chlorahololide D, and cycloshizukaol A. The planar structures of the new compounds were established by 1D-, 2D-NMR, and MS analyses. The absolute configurations of these compounds were determined by analyzing rotating Overhauser enhancement and exchange spectroscopy (ROESY) and circular dichroism (CD) spectra.     

Photochemical deprotection of nitro-substituted benzenesulfenates via photoinduced electron transfer

The photochemical deprotection of alkyl 2,4-dinitrobenzenesulfenate or alkyl 2-nitrobenzenesulfenate was successfully achieved by addition of triethylamine, while it was unsuccessful without triethylamine. The sulfur-oxygen bond cleavage is thought to occur heterolytically in the sulfenate anion radical produced by photoinduced electron transfer with triethylamine.     

A new synthesis of 7-substituted 2,3-bis(alkylthio)naphth[1,8-bc]-azepines using the tris(alkylthio)cyclopropenyl cation

7-Substituted 2,3-bis(isopropylthio)naphth[1,8-bc]azepines 3a-c were synthesized in good yields by the reactions of 5-substituted 1-naphthylamines 2a-c with tris(isopropylthio)cyclopropenylium perchlorate ( 1 ) in acetonitrile under reflux. This reaction proceeds through the facile ring opening of 1 , followed by the intermediary formation of iminium salts 5a-c and then intramolecular cyclization.     

Carbon chemical shifts of 1,1-diphenylethylene and α-methylstyrene dimer dianions

The natural abundance C-13 NMR spectra of 1,1-diphenylethylene and α-methylstyrene dimer dianions have been obtained using the proton noise decoupling technique. The extra negative charge distributions in the carbanions have been discussed and compared with those obtained from the proton chemical shifts. The chemical shifts of the two ortho carbons in a phenyl ring are equivalent to each other for the former carbanion but not for the latter.