Due to narrowband emission and high quantum efficiencies, polycyclic aromatic heterocycles with multi-resonance thermally activated delayed fluorescence (MR-TADF) properties have recently gained considerable attention in the organic optoelectronic field. Albeit their great promise in the full visible region covering from blue to red, MR-TADF emitters with ultraviolet emission have been rarely reported. Through locking the two ortho-positions of a triphenylamine core by sulfone groups, a simple polycyclic aromatic heterocycle, BTPT, was facilely constructed, exhibiting 368 nm ultraviolet emission with a narrow full width at half maximum (FWHM) of 33 nm. Its neat film exhibited distinct TADF property with a main emission peak at 388 nm. Noteworthily, the enantiomeric crystals of BTPT not only demonstrated significant circularly polarized luminescence (CPL) with large luminescence dissymmetry factor in the 10?3 order but also displayed obvious room temperature phosphorescence (RTP). The relationship between this innovative helical unit and unique photophysical properties, including ultraviolet MRTADF, CPL, and RTP, was reasonably revealed.
Non steroidal anti-inflammatory drugs are the most widely used medicines for relief of pain. These drugs have some side effects,
particularly toxicity in the gastrointestinal tract and kidneys. Various approaches have been used for obtaining safer anti-inflammatory
drugs. In this review we have summarized the recent developments in the following areas; (i) mode of action of NSAIDs (ii)
Role of COX-1 & COX-2 in inflammation, (iii) Different approaches used to improve gastric tolerance i.e. chemical manipulation,
formulation & co-administration, development of non specific (COX-1 & COX-2 inhibitors) and specific (COX-2 inhibitors) inflammation
inhibitors, and development of inflammation inhibitors having a mode of action other than COX-1 & COX-2 inhibition. We have
also focused on the safety of COX-2 inhibitors and the synthesis of heterocyclic compounds and their role as inflammation
inhibitors. 相似文献
An efficient cobalt-catalyzed carbocylization for the synthesis of indenols and indenes and a new method for reductive decyanation are described. 2-Iodophenyl ketones and aldehydes 1a-g undergo carbocyclization with various disubstituted alkynes 2a-k in the presence of Co(dppe)I(2) and zinc powder in acetonitrile at 80 degrees C for 3 h to afford the corresponding indenol derivatives 3a-s and4a-m in good to excellent yields. For some unsymmetrical alkynes, the carbocyclization was remarkably regioselective, affording a single regioisomer. The cobalt-catalyzed carbocyclization reaction was successfully extended to the synthesis of indene derivatives. Thus, the reaction of 2-iodophenyl ketones and aldehydes (1) with acrylates H(2)C=CHCO(2)R (7a-d) and acrylonitrile H(2)C=CHCN (7e) proceeds smoothly in the presence of Co(dppe)Cl(2)/dppe and zinc powder in acetonitrile at 80 degrees C for 24 h to afford the corresponding indenes 8a-k and 9a-c in moderate to good yields. Interestingly, when 7e was employed for the carbocylization, reductive decyanation also occurred to give an indene derivative without the cyano functionality. A possible mechanism for this cobalt-catalyzed carbocyclization reaction is also proposed. 相似文献
The goal of the present study is to test the hypothesis that LPA induces proliferation of astrocytes in hippocampus in vivo via phosphorylation of ERK 1/2. We first characterized the expression of GFAP, a special marker fiber protein of astrocytes,
in brain slices after direct injection of LPA into hippocampus by immunohistochemistry, and found that LPA induced a remarkable
proliferation of astrocytes. Then double-lablled immunofluorescence was used to detect GFAP and phosphorylation ERK 1/2 (p-ERK
1/2), LPA induced an immediate (10 min) and transient (<30 min) phosphorylation of ERK 1/2, and sequence sustained activation
of ERK 1/2 was observed, which last for at least 3 weeks after injection of LPA. Reactions are inhibited by U0126, a specific
pharmacological mitogen-activated protein kinase (MEK) inhibitor. Laser confocal scanning was used to study spatial relationship
of p-ERK and astrocytes. Amazingly, the early (<7 days) phosphorylation of ERK 1/2 is not expressed in astrocytes but in area
where neurons and/or in other cell type(s) occupied, expression of p-ERK 1/2 in astrocytes is not detected until 14 days after
LPA injection and lasts for at least 3 weeks. Taken together, these data suggest that LPA play an important role in proliferation
of astrocytes through phosphorylation of ERK 1/2 in hippocampus. It provides further proof for the functions of LPA in CNS
injury, and may contribute to clinical therapy for relative diseases. 相似文献
A high-performance capillary electrophoretic (CE) method with electrochemical detection (ED) has been developed for determination of the pharmacologically active flavonoids in Ginkgo biloba L. and phytopharmaceuticals containing its extract. Epicatechin, catechin, rutin, apigenin, luteolin, and quercetin are important flavonoids in this plant. Operated in a wall-jet configuration, a 300 micro m diameter carbon-disk electrode was used as working electrode with good response to the six analytes at +1000 mV (relative to the SCE). Under the optimum conditions, the analytes were separated within 22 min in a borax buffer (pH 9.0). Excellent linearity was obtained over two orders of magnitude and detection limits (S/N=3) ranged from 1.4 x 10(-7) to 5.0 x 10(-7) g mL(-1) for all six analytes. The method was successfully used for assay of Ginkgo biloba L. and its phytopharmaceuticals after a relatively simple extraction procedure; the results obtained were satisfactory. 相似文献
The reaction of o-bromobenzoate (1 b) with benzaldehyde (2 a) in the presence of [NiBr(2)(dppe)] (dppe=1,2-bis(diphenylphosphino)ethane) and zinc powder in THF (24 hours, reflux temperature), afforded 3-phenyl-3H-isobenzofuran-1-one (3 a) in an 86 % yield. Similarly, o-iodobenzoate reacts with 2 a to give 3 a, but in a lower yield (50 %). A series of substituted aromatic and aliphatic aldehydes (2 b, 4-MeC(6)H(4)CHO; 2 c, 4-MeOC(6)H(4)CHO; 2 d, 3-MeOC(6)H(4)CHO; 2 e, 2-MeOC(6)H(4)CHO; 2 f, 4-CNC(6)H(4)CHO; 2 g, 4-(Me)(3)CC(6)H(4)CHO; 2 h, 4-C(6)H(5)C(6)H(4)CHO; 2 i, 4-ClC(6)H(4)CHO; 2 j, 4-CF(3)C(6)H(4)CHO; 2 k, CH(3)(CH(2))(5)CHO; 2 l, CH(3)(CH(2))(2)CHO) also underwent cyclization with o-bromobenzoate (1 b) producing the corresponding phthalide derivatives in moderate to excellent yields and with high chemoselectivity. Like 1 b, methyl 2-bromo-4,5-dimethoxybenzoate (1 c) reacts with tolualdehyde (2 b) to give the corresponding substituted phthalide 3 m in a 71 % yield. The methodology can be further applied to the synthesis of six-membered lactones. The reaction of methyl 2-(2-bromophenyl)acetate (1 d) with benzaldehyde under similar reaction conditions afforded six-membered lactone 3 o in a 68 % yield. A possible catalytic mechanism for this cyclization is also proposed. 相似文献
Summary. 4-Aminobicyclo[2.2.2]octanones which were prepared in one-pot-reactions from benzylidene acetone and dialkylammonium rhodanides
were reduced stereoselectively to their corresponding alcohols. The activities of the bicyclic compounds against causative
organisms of tropical deseases were examined. The 4-aminobicyclo[2.2.2]octan-2-ols were in general more active against Trypanosoma b. rhodesiense and Plasmodium falciparum than the corresponding keto compounds.
Corresponding author. E-mail: robert.weis@uni-graz.at
Received November 27, 2002; accepted December 2, 2002
Published online May 2, 2003 相似文献
WO3 and WO3:P (5 mol% H3PO4) thin films were prepared using the sol-gel route and the electrochromic properties of the films were investigated using
in situ spectroelectrochemical methods. The measurements were performed in propylene carbonate solution with 0.1 M LiClO4 as electrolyte. During the cathodic polarization at –0.8 V a blue coloration is observed with a reversible variation between
14% and 84% of the transmittance at λ=633 nm. The kinetics for the bleaching process is faster for the WO3:P film than for the undoped WO3 film.
Electronic Publication 相似文献
The G3(MP2) method has been employed to study the 1,4-addition reactions between singlet oxygen and five acenes, including benzene, naphthalene, anthrecene, tetracene, and pentacene. In all, nine pathways between O(2) and the five acenes have been investigated. Our calculated results indicate that all nine pathways are concerted and exothermic and that the most reactive sites on the acenes are the center ring's meso-carbons. In addition, reactivity increases along the series benzene < naphthalene < anthrecene < tetracene < pentacene. This trend is identical to that of aromaticity for the five acenes. A correlation between reactivity and aromaticity is briefly rationalized with natural bond orbital (NBO) analysis and frontier molecular orbital (FMO) analysis. Furthermore, some experimental kinetics data from the literature supporting the calculated results are cited. 相似文献