A reexamination of Biginelli-like multicomponent condensation reaction: One-pot regioselective synthesis of spiro heterobicyclic rings

A pseudo four-component reaction is described, leading to the efficient regioselective synthesis of sigma symmetric spiro heterobicyclic rings using aldehydes and urea in the presence of cyclic beta-diester or beta-diamides such as Meldrum's acid or barbituric acid derivatives. The reaction needs no added catalyst and proceeds solvent-free conditions at 80 degrees C.     

Unexpected dimerization of 1,3‐dimethyl‐5‐methylenebarbituric acid revealed by a combined experimental and computational study

A comparison of experimental and calculated ¹³C‐nuclear magnetic resonance chemical shifts reveals the molecular structure of a dimer that was obtained by an unexpected dimerization of 1,3‐dimethyl‐5‐methylenebarbituric acid. Furthermore, the puckering angle of the cyclobutane unit linking the six‐membered rings is discussed in detail. The influence of substituents on 1,3‐position of the cyclobutane ring on the puckering angle is demonstrated based on 1,1,3,3‐tetramethylcyclobutane. Copyright © 2015 John Wiley & Sons, Ltd.     

聚合物薄膜中生色团分子间的相互作用对其宏观二阶非线性的影响

制备了3-(1,1-二氰基噻吩)-1-苯-4,5-二羟基-H-噻唑(DCNP)与聚醚醚酮(PEK-c)组成的主客掺杂聚合物薄膜,用Maker条纹法测量了不同掺杂浓度下薄膜的二阶非线性系数χ₃₃⁽²⁾.实验结果表明,聚合物中生色团的含量高到一定程度,其宏观二阶非线性随生色团含量的增加反而下降.本文在考虑聚合物中生色团分子相互作用的情况下,修正了聚合物宏观二阶非线性与生色团的含量之间的关系,此时聚合物宏观二阶非线性与生色团的含量已非简单的正比关系.讨论了生色团分子间 关键词：     

Uniqueness and wavelength optimization in continuous-wave multispectral diffuse optical tomography

We derive conditions for the unique and simultaneous recovery of chromophore concentrations and scattering coefficients in multispectral continuous-wave diffuse optical tomography. These conditions depend strongly on measurement wavelengths. We introduce and demonstrate a general methodology for choosing those wavelengths, which yields superior separation of scattering from absorption and superior separation of one chromophore from another. Application of these concepts should significantly improve the fidelity of continuous-wave diffuse near-infrared optical tomography in tissues.     

Structure, phase (aggregate) state, and optical properties of a new heat-resistant polymer with a nonlinear optical chromophore

A new heat-resistant copolymer (II) with a nonlinear optical chromophore in a side chain was synthesized by the etherification of side hydroxyl groups in chains of silicon-containing poly(o-hydroxyamide) (I) with 4′-{(6-chlorohexyl)methylamino}-4-nitroazobenzene (chromophore) under conditions of phase-transfer catalysis. The structure and phase (aggregate) states of copolymer II were investigated using x-ray diffraction and differential scanning calorimetry. It was shown that the substitution of chromophore molecules for up to 15% of hydrogen atoms in hydroxyl groups of amorphous copolymer I most likely leads to an independent arrangement of the chromophoric groups and the formation of crystal domains. It was established that this ordering substantially affects the stability and efficiency of the nonlinear optical properties of films prepared from copolymer II and is probably responsible for the slow decay of the second-harmonic generation signal in the sample.     

吡嗪-2-羧酸在γ-改性磷酸锆中的插层组装及发光性能

采用直接沉淀法制备了层状框架γ-磷酸锆（γ-ZrP）及改性磷酸锆（γ-DDZrP）,通过插层化学法将吡嗪-2-羧酸生色团与改性磷酸锆进行杂化组装。X射线衍射结果显示,γ-DDZrP的层间距（3.70 nm）远远大于γ-ZrP（1.11 nm）,这有利于吡嗪-2-羧酸生色团的插入。组装后层状框架的层间距由3.70 nm减小为3.33~3.29 nm。 荧光光谱表明,最大发射峰位置发生了明显蓝移,由溶液中的373 nm蓝移至悬浮液的366 nm。研究发现,吡嗪-2-羧酸在水溶液中的荧光强度很低,但形成插层组装后,悬浮液的荧光强度有了很大程度的提高,当浓度为15 μmol/L时,荧光强度增大了6倍。这说明γ-DDZrP能够改善吡嗪-2-羧酸的荧光性能,有利于其在分子识别和荧光探针等领域的应用。     

Fluorescence Study on the Structure of Ionic Liquid Aggregates in Aqueous Solutions

Although ionic liquids are a relatively novel class of materials, it is well documented that they form micelles through aggregation of cation aliphatic tails. However, anion self-assembly has not yet been reported. In this study, we analyzed the intrinsic fluorescence of p-toluenesulfonate groups (tosylate) as part of the ionic liquid 1-ethyl-3-methylimidazolium tosylate ([emim][TOS]) and p-toluenesulfonic acid (pTSA), in aqueous solution. pTSA was found to have overlapping monomer and excimer emissions for chromophore concentrations from 10⁻³ to 1 M, whereas [emim][TOS], in the same conditions, showed monomer emission slightly broadened by much weaker excimer emission. These different photophysical behaviors of the same chromophore in the two compounds are explained by the formation of ion pairs by [emim][TOS], which can also be inferred from the loss of vibrational structure of the absorption spectra with respect to pTSA. Despite this different behavior regarding ion pairing, anion aggregation was observed in the excitation spectra of both pTSA and [emim][TOS]. While the absorption spectra corresponded to single chromophores, the excitation spectra changed from those characteristic of a single chromophore (below 10⁻³ M) to red-shifted narrow bands (above 0.1 M) typical of J aggregates. Between those concentrations, the excitation spectra split into blue- and red-shifted bands with relative intensities that changed with concentration as the chromophores rearranged in their clusters from head-to-head to head-to-tail aggregates. Differences between the absorption and excitation spectra were ascribed to aggregation-induced fluorescence enhancement.     

Direct four-photon excitation of amplified spontaneous emission in a nonlinear organic chromophore

We report four-photon pumped amplified spontaneous emission in an organic chromophore. The phenomenon is observed when intense infrared laser radiation illuminates a nonlinear chromophore solution. As a result of this illumination, a strong and highly directional radiation in the visible wavelength range is generated in both the forward and the backward directions, with an angular divergence similar to that of the pump beam.     

Chromophores of the green fluorescent protein studied in the gas phase

Absorption of gas-phase biomolecules has been studied at the heavy-ion storage ring ELISA. Here we discuss the absorption characteristics of the chromophores of the Green Fluorescent Protein (GFP). The gas-phase absorption maximum of the deprotonated chromophore (anion form) is at 479 nm. This is almost identical to one of the two absorption maxima of the protein, being at 477 nm, which is ascribed to a deprotonated chromophore in the protein. The protonated chromophore (cation form) has a maximum at 406 nm in the gas phase. We compare the gas-phase results with absorption profiles of GFP and chromophores in liquids, and argue that the absorption characteristics of GFP are mainly ascribed to intrinsic chemical properties of the chromophore. Evidently, the special β-can structure of GFP provides shielding of the chromophore from the surroundings without significantly changing the electronic structure of the chromophore through interactions with amino acid side chains. Received 28 December 2001 Published online 13 September 2002     

Relations between photophysical and lasing properties of rhodamines in solid polymeric matrices

2 laser) pulses. In these solid media the rhodamine chromophore shows a photophysical behaviour similar to that in a liquid solution, and its photostability clearly increases when the chromophore is bound to the polymeric chain. These new solid materials show laser efficiencies that depend on the HEMA/MMA ratio, in some cases with values close to 20%. Received: 15 May 1996/Revised version: 26 November 1996     

Stimulated Electron Spin Polarization in Strongly Coupled Triplet–Doublet Spin Pairs

The possibility of stimulating electron spin polarization in a system consisting of a stable paramagnetic center and a chromophore that can be excited into its triplet state is discussed. In such systems, the doublet state of the paramagnetic center couples to the excited triplet state of the chromophore and if the coupling is larger than the difference in the precession frequencies of the doublet and triplet, the eigenstates of the coupled system are quartet and doublet states. The quartet state is usually the lowest energy excited state. Following light excitation, the initial electronic relaxation to the quartet state generates strong multiplet polarization if it is governed by the spin–orbit coupling that follows the molecular symmetry. It is shown that application of a selective π-pulse to the ±3/2 ↔ ±1/2 transitions of the quartet converts this multiplet polarization into net polarization. The magnitude and orientation dependence of the generated polarization is estimated on the basis of a simple analytical model. The experimental conditions required for this net polarization to be retained in the ground state after decay of the quartet state are discussed. The viability of using this as a method to enhance the signal strength of a spin label or metal center in selective excitation experiments is considered.     

Optimization of spectral sensitivities of mosaic five-band camera for estimating chromophore densities from skin images including shading and surface reflections

Optical Review - In this paper, the spectral sensitivities of a mosaic five-band camera were optimized using a numerical skin phantom to perform the separation of chromophore densities, shading and...     

Single-layered photovoltaics based on cyano-substituted pyrazoloquinoline chromophores

The efficiency of a single-layered photovoltaic (PV) cell was increased by up to 44% by using cyano-substituted pyrazoloquinoline chromophores. The role of the incorporated chromophore in changing the effective exciton radius formed by Coulombic chromophore–polymer interactions was analyzed using density functional theory (DFT) quantum chemical simulations. Both the ground-state dipole moments of chromophore, as well as their electrostatic interactions with the conjugated conducting polymer chains, are shown to play an important role. In particular, incorporation of the highly polarised cyano group leads to enhancement of the ground-state dipole moments and enables an open-circuit voltage up to 1.107 V, an enhancement of at least 40% compared to pyrazoloquinoline without cyano groups. At the same time, the exciton length determined by chromophore–matrix interactions and polaronic effects demonstrate a stronger correlation with the observed PV efficiencies.     

Excitation energy transfer in chromophore aggregates within a dissipative medium

The Redfield theory-based model of excitation energy transfer in chromophore ensembles within dissipative environment is proposed. Application of the multipole expansion to an operator of interaction between the chromophore molecules and the environment together with some assumptions about the latter led to the closed-form expressions for the elements of the dissipation tensor. These expressions relate the rates of transition between eigenstates of a chromophore ensemble with the spectral and electronic properties of an environment and the chromophore molecules. For several model cases the exact solution of the Redfield equations was obtained.     

Detection of Free Thiols and Fluorescence Response of Phycoerythrin Chromophore after Ultraviolet-B Radiation Stress

The chemistry of thiol-chromophore linkage plays a central role in the nature of fluorescence of phycoerythrin (PE). Interaction of thiol and chromophore is crucial for the energy transfer, redox signal and inhibition of oxidative damage. In the present investigation the effects of ultraviolet-B radiation on an emission fluorescence intensity and wavelength shift in PE due to interaction between thiol and chromophore by remarkable strategy of detection technique was studied. Purification of PE was done by using a gel permeation and ion exchange chromatography that yielded a quite high purity index (6.40) in a monomeric (αβ) form. UV-B radiation accelerated the quenching efficiency (24.9 ± 1.52%) by reducing fluorescence emission intensity of thiol linked chromophore after 240 min of UV-B exposure. However, after blocking of transiently released free thiol by N-ethylmaleimide, quenching efficiency was increased (36.8 ± 2.80%) with marked emission wavelength shift towards shorter wavelengths up to 562 nm as compared to 575 nm in control. Emission fluorescence of free thiol was at maximum after 240 min that was detected specifically by monobromobimane (mBrB) molecular probe. The association/dissociation of bilin chromophore was analyzed by SDS- and Native-PAGE that also indicated a complete reduction in emission fluorescence. Our work clearly shows an early detection of free thiols and relative interaction with chromophore after UV-B radiation which might play a significant role in structural and functional integrity of terminal PE.     

Steady-State and Time-Resolved Fluorescence Polarization Behavior of Acenaphthene

Steady-state and time-resolved fluorescence polarization studies have been carried out on acenaphthene (ACE) in low-temperature glass solutions and at room temperature. In the low-temperature glass the fluorescence polarization values vary considerably with both emission and excitation wavelength. There is a time dependence (on the nanosecond time scale) of the fluorescence anisotropy, r(t), at 77 K, which has a strong dependence upon the excitation and emission wavelengths. Under these conditions, the time-dependent decay of the anisotropy is not attributable to chromophoric motion. The observations are consistent with emission from two closely lying and interconverting excited states. Rate constants for the photophysical processes involved have been determined by fitting the data using a model proposed by Fleming et. al. The results are discussed with particular reference to the care required in using dynamic fluorescence polarization measurements to determine energy transfer rates in systems containing this chromophore.     

Magnetic brillouin zone effect on the resistivity of semimetallic-like fermi surface in USb

To probe the effect of the protein environment on the retinal chromophore of rhodopsin, we performed molecular dynamics simulations using combined quantum mechanics/molecular mechanics (QM/MM). The starting geometry of the protein is based on the 2.6Å X-ray structure of bovine rhodopsin of Okada et al. [T. Okada, et al. Proc. Natl. Acad. Sci. USA 99 5982 (2002)]. The wild-type chromophore of rhodopsin according to our calculations shows a highly twisted conformation around the central region, from C10 to C13, due to non-bonded interaction with the protein pocket. The absolute sense of twist of the C11–C12 and C12–C13 bonds is negative (?19 ± 9°) and positive (170 ± 8°), respectively. The 13-demethyl retinal chromophore, in which the methyl group at the C13 position is removed, is less distorted in this region. The C11–C12 bond is less twisted (?15 ± 10°) and the C12–C13 bond is planar (179 ± 9°) . The flattened geometry of this artificial chromophore is supported by spectroscopic evidence.     

Luminescence kinetics of linear polymer molecules with chromophores regularly distributed along the chain

An analytical expression for luminescence kinetics of a polymer chain in the static regime is obtained for the case when the rotational motion of monomers, leading to the formation of excimers (traps of excitations), is frozen. The conditions are found when the inhomogeneous broadening of the chromophore spectra and the conformation motion of the polymer chain should be taken into account.     

Non-lorentzian single-molecule line shape: pseudolocal phonons and coherence transfer

The excitation line shape of a single terrylene molecule in a naphthalene crystal has been investigated. In addition to the conventional Lorentzian, it consists of a dispersive component in the core region and a sideband. This is due to a pseudolocal phonon caused by the substitution of a host molecule with the chromophore. When the pseudolocal phonon is excited, the resonance frequency of the chromophore slightly changes, resulting in the appearance of a second, quasiresonant transition. Coherence transfer between these two optical transitions causes the deviation from the purely Lorentzian line shape.     

Retinal in bacteriorhodopsin and related molecular models investigated with Raman spectroscopy and density functional theory calculations

A first‐principles assisted study of the Raman spectrum associated with the photoactive chromophore in bacteriorhodopsin (bR) allowed the elucidation of the effective coupling existing between the π electrons of the retinylidene chromophore and the local environment of the Schiff base. The role of the counter‐ion on the electronic and vibrational structure of the chromophore is investigated by means of density functional theory (DFT) calculations. Several molecular models of the retinylidene chromophore interacting with different counter‐ions facing the Schiff base have been considered. The counter‐ion induces a strong modulation of the position of both the UV–vis absorption maximum and the strong Raman active collective CC stretching mode, related to the effective conjugation coordinate (ECC). Experimental Raman and UV–vis absorption data are interpreted in the light of these theoretical findings. The data collected in this paper provide an interesting accumulation of points along the optical gap versus ECC wavenumber relationship. Copyright © 2011 John Wiley & Sons, Ltd.