scholarly journals Heterocyclic aldehydes based on thieno[3,2-<em>b</em>]thiophene core: synthesis and preliminary studies as ion optical chemosensors

2020 ◽  
Author(s):  
Manuela Raposo ◽  
Rui Sousa ◽  
Raquel Gonçalves ◽  
Susana Costa ◽  
Rita Figueira
Chemosensors ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 1
Author(s):  
Miao Zhang ◽  
Jiangfan Shi ◽  
Chenglong Liao ◽  
Qingyun Tian ◽  
Chuanyi Wang ◽  
...  

Perylene imide (PI) molecules and materials have been extensively studied for optical chemical sensors, particularly those based on fluorescence and colorimetric mode, taking advantage of the unique features of PIs such as structure tunability, good thermal, optical and chemical stability, strong electron affinity, strong visible light absorption and high fluorescence quantum yield. PI-based optical chemosensors have now found broad applications in gas phase detection of chemicals, including explosives, biomarkers of some food and diseases (such as organic amines (alkylamines and aromatic amines)), benzene homologs, organic peroxides, phenols and nitroaromatics, etc. In this review, the recent research on PI-based fluorometric and colorimetric sensors, as well as array technology incorporating multiple sensors, is reviewed along with the discussion of potential applications in environment, health and public safety areas. Specifically, we discuss the molecular design and aggregate architecture of PIs in correlation with the corresponding sensor performances (including sensitivity, selectivity, response time, recovery time, reversibility, etc.). We also provide a perspective summary highlighting the great potential for future development of PIs optical chemosensors, especially in the sensor array format that will largely enhance the detection specificity in complexed environments.


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 287
Author(s):  
Jianguo Liu ◽  
Mingyue Zhang ◽  
Longlong Ma

Dibenzylamine motifs are an important class of crucial organic compounds and are widely used in fine chemical and pharmaceutical industries. The development of the efficient, economical, and environmentally friendly synthesis of amines using transition metal-based heterogeneous catalysts remains both desirable and challenging. Herein, we prepared the covalent organic framework (COF)-supported heterogeneous reduced COF-supported Pd-based catalyst and used it for the one-pot reductive amination of aldehydes. There are both Pd metallic state and oxidated Pdσ+ in the catalysts. Furthermore, in the presence of the reduced COF-supported Pd-based catalyst, many aromatic, aliphatic, and heterocyclic aldehydes with various functional groups substituted were converted to their corresponding amines products in good to excellent selectivity (up to 91%) under mild reaction conditions (70 °C, 2 h, NH3, 20 bar H2). This work expands the covalent organic frameworks for the material family and its support catalyst, opening up new catalytic applications in the economical, practical, and effective synthesis of secondary amines.


2012 ◽  
Vol 9 (4) ◽  
pp. 1897-1905 ◽  
Author(s):  
A. Solankee ◽  
K. Patel ◽  
R. Patel

Chalcones(6a-f)have been prepared by the condensation of ketone(5)and different aromatic and heterocyclic aldehydes. These chalcones(6a-f)on treatment with guanidine hydrochloride and phenyl hydrazine hydrochloride in presence of alkali give aminopyrimidines(7a-f)and phenylpyrazolines(8a-f)respectively. All the newly synthesized compounds have been characterized on the basis of IR,1HNMR spectral data as well as physical data. Antibacterial activity (minimum inhibitory concentration MIC) against Gram-positiveS. aureusMTCC 96 andS. pyogeneusMTCC 442 and Gram-negativeP. aeruginosaMTCC 1688 andE. coliMTCC 443 bacteria, as well as antifungal acivities (MIC) againstC. albicansMTCC 227,A. nigerMTCC 282 andA. clavatusMTCC 1323 were determined by broth dilution method.


2021 ◽  
Vol 317 ◽  
pp. 202-207
Author(s):  
Juan Matmin ◽  
Nur Fatiha Ghazalli ◽  
Fazira Ilyana Abdul Razak ◽  
Hendrik O. Lintang ◽  
Mohamad Azani Jalani

The scientific investigation based on the molecular design of aromatic compounds for high-performance chemosensor is challenging. This is because their multiplex interactions at the molecular level should be precisely determined before the desired compounds can be successfully used as sensing materials. Herein, we report on the molecular design of chemosensors based on aromatic structures of benzene as the organic motif of benzene-1,3,5-tricarboxamides (BTA), as well as the benzene pyrazole complexes (BPz) side chain, respectively. In the case of BTA, the aromatic benzene acts as the centre to allow the formation of π–π stacking for one-dimensional materials having rod-like arrangements that are stabilized by threefold hydrogen bonding. We found that when nitrate was applied, the rod-like BTA spontaneously formed into a random aggregate due to the deformation of its hydrogen bonding to form inactive nitroso groups for non-optical sensing capability. For the optical chemosensor, the aromatic benzene is decorated as a side-chain of BPz to ensure that cage-shaped molecules make maximum use of their centre providing metal-metal interactions for fluorescence-based sensing materials. In particular, when exposed to benzene, Cu-BPz displayed a blue-shift of its original emission band from 616 to 572 nm (Δ = 44 nm) and emitted bright orange to green emission colours. We also observe a different mode of fluorescence-based sensing materials for Au-BPz, which shows a particular quenching mechanism resulting in 81% loss of its original intensity on benzene exposure to give less red-orange emission (λ = 612 nm). The BTA and BPz synthesized are promising high-performance supramolecular chemosensors based on the non-optical and optical sensing capability of a particular interest analyte.


2015 ◽  
Vol 77 (3) ◽  
Author(s):  
Helmi Mohammed Al-Maqtari ◽  
Joazaizulfazli Jamalis ◽  
Hasnah Mohd Sirat

Heterocyclic chalcones containing halogenated thiophenes were synthesized. The first step was to synthesize 3-acetyl-2,5-dichlorothiophene and 2-acetyl-5-chlorothiophene as heterocyclic ketones by using Friedel-Crafts acylation. The ketones were then used to synthesize thiophene chalcones through Claisen-Schmidt reaction with the respective heterocyclic aldehydes such as 5-bromothiophene-2-carbaldehyde, 3-methyl-2-thiophene carboxaldehyde and 2-thiophene carboxaldehyde with 3-acetyl-2,5-dichlorothiophene or 2-acetyl-5-chlorothiophene in presence of basic medium, sodium hydroxide to form the corresponding chalcones. Structures of the synthetic compounds were confirmed by IR, MS, 1H and 13C NMR spectral data.


2019 ◽  
Vol 15 (1) ◽  
pp. 82-87
Author(s):  
Alexandra Alexandrovna Kudrevatykh ◽  
Lyubov Stepanovna Klimenko ◽  
Timofey Petrovich Martyanov

Molecular interactions with various anions in the form of tetrabutylammonium salts in DMSO and DMSO-aqueous mixture were studied spectrophotometrically. It turned out that the solutions of 1-hydroxy-2-acylaminoanthraquinones in DMSO, originally yellow, became dark purple with the addition of cyanide, fluoride, phosphate, and acetate ions. The addition of other salts did not cause changes in the absorption spectra. When switching to aqueous DMSO, a contrasting color change in the solution was observed only with the addition of the cyanide ion. The stability constants of the complexes and the metrological characteristics of the processes were determined. On the basis of 1hydroxy-2-benzoylaminoanthraquinone, colorimetric test strips were made and tested for the detection of CN-ions in an aqueous medium.


1975 ◽  
Vol 6 (18) ◽  
pp. no-no
Author(s):  
I. SCHWARTZ ◽  
R. D. POP ◽  
H. DEMIAN ◽  
ANA MURESAN ◽  
ELENA CHINDRIS ◽  
...  

2019 ◽  
Vol 1 (7) ◽  
pp. 1757-1768 ◽  
Author(s):  
Rafaela I. Stock ◽  
Juliana P. Dreyer ◽  
Gisele E. Nunes ◽  
Ivan H. Bechtold ◽  
Vanderlei G. Machado

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