Isolation, characterization, and reaction of activated iodosylbenzene monomer hydroxy(phenyl)iodonium ion with hypervalent bonding: supramolecular complex PhI+OH.18-crown-6 with secondary I...O interactions

The isolation, characterization, and reaction of the active species hydroxy(phenyl)iodonium ion with hypervalent bonding are reported. Reaction of iodosylbenzene with HBF(4)-Me(2)O in the presence of equimolar 18-crown-6 in dichloromethane afforded the hydroxy-lambda(3)-iodane complex PhI(OH)BF(4).18-crown-6 as stable yellow prisms. X-ray structure analysis indicated that both the close contacts between the iodine(III) and the three adjacent oxygen atoms of 18-crown-6, and the hydrogen bonding OH.O(crown ether) will be responsible for the increased stability of the complex as compared to the uncomplexed PhI(OH)BF(4). The crown ether complex is highly reactive and serves as a versatile oxidant even in water: thus, the complex undergoes oxidative transformations of a variety of functional groups such as olefins, alkynes, enones, silyl enol ethers, sulfides, and phenols under mild conditions.     

Multireference configuration interaction calculations for positronium halides

Multireference configuration interaction (MRCI) calculations of the positronium halides, PsF, PsCl, PsBr, and PsI, are carried out, to give positron ionization energies, positronium binding energies, and two-photon annihilation rates. All CI calculations consider only valence correlation effect with a frozen-core approximation, and use the orbitals with angular momentum up to 8. To incorporate the effects of many-body correlations in the energies and two-photon annihilation rates, the MRCI calculations are repeated with increasing reference configurations, and the full CI limits of these energies and annihilation rates are estimated. The contribution from orbitals having angular momentum greater than 8 to those values is also estimated. Relative to our previous single reference CI calculations, many-body correlation effects significantly increase the positron ionization energies, positronium binding energies, and two-photon annihilation rates. The structures of the positronium halides are also discussed.     

Large optical nonlinearity of semiconducting single-walled carbon nanotubes under resonant excitations

We measured third-order nonlinear susceptibility (chi(3)) spectra in semiconducting single-walled carbon nanotubes (SWNTs) by the Z-scan method. |Imchi(3)| is remarkably enhanced under resonant excitation to the lowest interband transition, reaching 4.2 x 10(-6) esu and 1.5 x 10(-7) esu in SWNTs grown by the laser ablation and HiPco methods, respectively. A comparison of the transient absorption changes evaluated by degenerate and nondegenerate pump-probe measurements suggests that the resonant enhancement of |Imchi(3)| is dominated by a coherent process rather than by saturation of absorption.     

Phase-locked widely tunable optical single-frequency generator based on a femtosecond comb

We present an arbitrary optical single-frequency generator based on a femtosecond optical frequency comb. The functions of this device are comparable to those of a radio-frequency synthesizer. However, this device operates at hundreds of terahertz. The absolute frequency accuracy of this synthesizer is approximately 1 kHz at a 282 THz carrier frequency. The stability is approximately 2 x 10(-14) at 100 s, and the tuning speed exceeds 30 GHz/s. This source demonstrates the integration of a phase-locked optical comb into a versatile and easy-to-use system for the generation of tunable, absolute optical frequencies. By using downconversion, one could generate tunable terahertz frequencies that are phase locked to a microwave reference, such as a Cs atomic clock, and high-precision interferometry could benefit greatly from the stability and accuracy of this widely tunable source.     

Highly regio- and stereoselective hydrostannylation of alkynols with a new Lewis acidic hydrostannane

[reaction: see text] Bu2Sn(OTf)H (1a), easily prepared from Bu2SnH2 and TfOH, was found to be very valuable for highly regio- and stereoselective hydrostannylation of various propargyl alcohols leading to (Z)-gamma-stannylated allyl alcohols. The stannylation with 1a is applicable to the synthesis of hydroxy-substituted (Z)-vinylstannanes from terminal alkynes bearing a hydroxy group at the homoallylic or bishomoallylic position. The coordination of the hydroxy group to the Lewis acidic tin center plays an important role for the observed regio- and stereochemistry.     

Hydrogen-bonding effects on the fluorescence versus electron-transfer-initiated chemiluminescence spectra of the m-oxybenzoate ion derived from a bicyclic dioxetane

A comparative spectral study of the fluorescence of the m-oxybenzoate anion versus the electron-transfer-initiated chemiluminescence (CIEEL) of the same anion derived from the bicyclic dioxetanes in various solvents is reported. The present study reveals that the fluorescence of this oxyanion is blue-shifted in protic versus aprotic solvents, while the CIEEL-spectral maximum is independent of the medium. The same phenomenon has been recently observed for the m-oxybenzoate ion derived from CIEEL-active spiroadamantyl dioxetanes. The reported spectral differences between the fluorescence and chemiluminescence emissions cannot be attributed to exciplex formation in the CIEEL process, but result from the differences in hydrogen-bonding effects on the photo- and chemiexcited oxyanion species. The observed solvatochromism is qualitatively rationalized in terms of the semiempirical AM1 calculations.     

Structure and stereochemistry of the higher bile acid isolated from turtle bile: (22S,25R)-3 alpha,12 alpha,15 alpha,22-tetrahydroxy-5 beta-cholestan-26-oic acid

The structure and stereochemistry of the higher bile acid, tetrahydroxyisosterocholanic acid (TISA), which was previously isolated from the bile of Amyda japonica (turtle) and proposed as a tetrahydroxyisosterocholanic acid, have been established as (22S,25R)-3 alpha,12 alpha,15 alpha,22-tetrahydroxy-5 beta-cholestan-26-oic acid by X-ray crystallographic analysis of its ethyl ester.     

Newly developed encapsulation-dehydration protocol for plantcryopreservation

A simplified and efficient encapsulation-dehydration protocol, which is a compromise between vitrification and encapsulation-dehydration, was presented for plant cryopreservation. In this protocol, during the encapsulation process, the apices precultured with 0.3 M sucrose for 16 h were simultaneously osmoprotected with a mixture of 02 M glycerol plus 0.4 M sucrose for 1 h. These encapsulated apices were directly dehydrated with dry silica gel prior to a plunge into LN without the pretreatment of 0.8M sucrose for 16 h. This protocol produced much higher rates of recovery growth in the three plant species tested (wasabi, chrysanthemum, and mint) than those cryopreserved by the conventional encapsulation-dehydration. This protocol also considerably reduced the time needed for the cryogenic procedure. Thus, this new protocol appears promising for cryopreservation of shoot apices and other explants.