Acridine N-Heterocyclic Carbene Gold(I) Compounds: Tuning from Yellow to Blue Luminescence

The synthesis and the luminescence features of three gold(I)-N-heterocyclic carbene (NHC) complexes are presented to study how the n-alkyl group can influence the luminescence properties in the crystalline state. The mononuclear gold(I)-NHC complexes, [( L¹ )Au(Cl)] ( 1 ), [( L² )Au(Cl)] ( 2 ), and [( L³ )Au(Cl)] ( 3 ) were isolated from the reactions between [(tht)AuCl] and corresponding NHC ligand precursors, [N-(9-acridinyl)-N’-(n-butyl)-imidazolium chloride, ( L¹ .HCl)], [N-(9-acridinyl)-N’-(n-pentyl)-imidazolium chloride, ( L² .HCl)] and [N-(9-acridinyl)-N’-(n-hexyl)-imidazolium chloride, ( L³ .HCl)]. Their single-crystal X-ray analysis reveals the influence of the n-alkyl groups on solid-state packing. A comparison of the luminescence features of 1 – 3 with n-alkyl substituents is explored. The molecules 1 – 3 depicted blue emission in the solution state, while the yellow emission (for 1 ), greenish-yellow emission (for 2 ), and blue emission (for 3 ) in the crystalline phase. This paradigm emission shift arises from n-butyl to n-pentyl and n-hexyl in the crystalline state due to the carbon-carbon rotation of the n-alkyl group, which tends to promote unusual solid packing. Hence n-alkyl group adds a novel emission property in the crystalline state. Density Functional Theory and Time-Dependent Density Functional Theory calculations were carried out for monomeric complex, N-(9-acridinyl)-N’-(n-heptyl)imidazole-2-ylidene gold(I) chloride and dimeric complex, N-(9-acridinyl)-N’-(n-heptyl)imidazole-2-ylidene gold(I) chloride to understand the structural and electronic properties.     

Manipulating Slow Magnetic Relaxation by Light in a Charge Transfer {Fe2Co} Complex

Some cyanide-bridged complexes are known for exhibiting slow magnetic relaxation behavior in a light-induced metastable state. Herein, an unexpected reverse effect is observed for the first time in the S= {Fe^II_LS-Co^III_LS-Fe^III_LS} (HS=high spin, LS=low spin) ground state of a novel V-shaped trinuclear cyanide-bridged {Fe₂Co} complex. In this complex, light-switchable iron-cobalt charge transfer with repeatable off/on switching of slow magnetic relaxation is discovered upon alternating laser irradiation at 785 and 560 nm. An important characteristic of the present compound is that the S= ground state exhibits slow magnetic relaxation before irradiation, whereas this is accelerated after irradiation. This is different from the typical behavior, where the light-induced metastable state exhibits slow magnetic relaxation.     

Detection and evaluation of security features embedded in paper using spectral-domain optical coherence tomography

We propose a new method for authenticating valuable paper sheets such as gift coupons, tickets, and cheques with the use of optical coherence tomography (OCT). This method is based on the detection and evaluation of cross-sectional structural characteristics of valuable paper sheets provided with security features. Commonly used as a security feature is a security thread, which is embedded in such paper sheets. In this paper, the nondestructive detection of the embedded security thread is demonstrated using spectral-domain OCT. The results showed that the security thread was clearly visualized in the OCT image despite the highly scattering nature of papers.     

Pressure-induced structure change of molten KCl

Abstract

Energy-dispersive X-ray diffraction experiments of molten KCl under high pressure have been carried out by using synchrotron radiation. The diffraction profiles of molten KCl were acquired just above the melting temperature of KCl up to 4 GPa. The reduced structure factor S(Q)'s for molten KCl do not show any change in their primary features, except for a gradual increase in the first peak intensity with increasing pressure. This implies that molten KCl does not show a first-order phase transition, such as the B1-B2 transition, found in solid KCl, but that the local structure in molten KCl must be changed by compression. According to a molecular-dynamics simulation, this change of S(Q) can be explained by a continuous increase in the coordination number of the nearest-neighbor ions in molten KCl with pressure.     

Enhanced photochemical‐shift of reflection band from an inverse opal film based on larger birefringent polymer liquid crystals: Effect of tolane group on the photochemical shift behavior

Photo‐chemically tunable photonic band gap materials are prepared by infiltration of liquid crystal polymers having azobenzene groups into voids of SiO₂ inverse opal films. Linearly polarized (LP) light irradiation results in transformation from a random to an anisotropic molecular orientation of azobenzene side chains in the voids of the SiO₂ inverse opal film, leading to the reversible and stable shift of the reflection peak to longer wavelength more than 15 nm. To improve switching properties, we use copolymers of azobenzene monomer and tolane monomer, which have higher birefringence, as infiltration materials into the voids. The azobenzene‐tolane copolymers are found to show higher birefringence than azobenzene homopolymers by the LP light irradiation at higher temperature. Consequently, the reflection band of the SiO₂ inverse opal film infiltrated with the azobenzene‐tolane copolymer can be shifted to longer wavelength region more than 55 nm by the irradiation of LP light. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1981–1990, 2009     

Stereoselective synthesis of 3-deoxy-piperidine iminosugars from l-lysine

A new method using electrochemical oxidation and/or OsO₄ oxidation has been used for the stereoselective synthesis of 2,3,6-trihydroxylated (5S)-piperidine derivatives. The electrochemical method was successively used for the conversion of N-protected piperidines to N-protected 1-methoxypiperidines and for the conversion of 2,3-didehydro-1-methoxypiperidine derivatives to 2,3-trans-1,2,3-triacetoxypiperidine derivatives. These triacetates were easily transformed into (2S,3S)-6-triacetoxy-(5S)-methylpiperidine and (2R,3R)-6-triacetoxy-(5S)-methylpiperidine. In addition, the 2,3-cis-dihydroxylation of 2,3-didehydro-1-methoxypiperidine derivatives with OsO₄ afforded (2R,3S)-6-triacetoxy-(5S)-methylpiperidine and (2S,3R)-6-triacetoxy-(5S)-methylpiperidine.