131525-50-3Relevant articles and documents
Investigation of iron(III) ionic structural complexes for seebeck coefficient enhancement using variation of ligand lengths with extended Π-conjugated bipyridyl ligands
Ibrahim, N.M.J. Nik,Said, S. Mohd,Mainal,Sabri, M.F. Mohd,Abdullah,Hasnan, M.M.I. Megat,Amin, N.A.A. Mohd,Salleh, M.F. Mohd
, (2021)
Five new octahedral spin-crossover magnetic complexes with general formulae, [Fe(LCn)3](BF4)3, where L = ligand, and n = 8, 10, 12, 14, 16, were synthesized and characterized. The influence of different ligand lengths on t
Synthesis, characterization and electrochemistry of polycyclic fused aromatic pyrroles and their conjugated polymers
Bhanvadia, Viraj J.,Mankad, Yash J.,Patel, Arun L.,Zade, Sanjio S.
, p. 13565 - 13572 (2018)
Polycyclic fused aromatic pyrrole-based compounds, benzodipyrrole, naphthobipyrrole and their alkylated derivatives, were synthesized and studied electrochemically. Amongst these, naphthobipyrrole having a tetracyclic fused aromatic structure was electrochemically polymerized to give the homopolymer of naphthobipyrrole, poly(naphthobipyrrole), indicating good reactivity of α,α′-pyrrolic positions towards oxidative coupling. As a strategic approach towards the synthesis of copolymers, naphthobipyrrole was copolymerized with arylaldehyde to afford poly(arylmethylene naphthobipyrrole) by exploring the reactivity of β,β′-pyrrolic positions. Moreover, optical and electrochemical studies showed that the copolymer possessed a low optical bandgap and an elevated HOMO level. The scan rate dependent cyclic voltammetry studies of the copolymer film showed the formation of an electroactive material.
Molecular design strategies for spin-crossover (SCO) metal complexes (Fe(II) and Co(II)) for thermoelectricity
Abdullah, N.,Che Hassan, H.,Mainal, A.,Megat Hasnan, M. M. I.,Mohd Sabri, M. F.,Mohd Salleh, M. F.,Nik Ibrahim, N. M. J.,Said, S. Mohd,Wan Mohd Mahiyiddin, W. A.
, (2020)
TEC are developing technology to generate electricity from thermal energy. It causes current flow when redox solution disturbs the electrochemical potential equilibrium between the electrolyte and two inert electrodes upon application of a temperature gra
Synthesis, mesomorphism, photophysics and device performance of liquid-crystalline pincer complexes of gold(iii)
Parker, Rachel R.,Liu, Denghui,Yu, Xiankang,Whitwood, Adrian C.,Zhu, Weiguo,Williams,Wang, Yafei,Lynam, Jason M.,Bruce, Duncan W.
supporting information, p. 1287 - 1302 (2021/02/12)
Emissive gold(iii) complexes of pincer 2,6-diphenylpyridines also bearing a phenylacetylide ligand have been modified at both the pincer and phenylacetylide to confer liquid crystalline properties, with most complexes showing a columnar hexagonal phase in
Synthesis and mesomorphic characterization of some novel steroidal mesogens: A structure–property correlation
Bhat S, Vanishree,Kumar, Sandeep,Raghunathan, V. A.
, (2021/08/25)
The steroidal derivatives are found to be extremely good mesogens since their inception. Because of their inherent chirality, they have the potential to induce a wide variety of liquid crystalline phases, including frustrated phases depending upon the structure of the steroidal skeleton and the substituents attached. In this report, a series of novel monoalkoxy and dialkoxy benzoate derivatives of ergosterol and a few monoalkoxy derivatives of stigmasterol have been synthesized and their mesomorphic property has been investigated. The derivatives exhibited various mesophases including SmA, SmC*, N*, TGB and blue phases. Also, the gelation ability of some of these derivatives with various organic solvents has been examined. Furthermore, the mesomorphism of these derivatives has been compared with the analogous cholesteryl counterparts.
Columnar self-assembly, electrochemical and luminescence properties of basket-shaped liquid crystalline derivatives of Schiff-base-moulded: P-tert -butyl-calix[4]arene
Sharma, Vinay S.,Sharma, Anuj S.,Worthington, Sheena J. B.,Shah, Priyanka A.,Shrivastav, Pranav S.
supporting information, p. 20610 - 20619 (2020/12/28)
A new family of supramolecular liquid crystalline compounds with a calix[4]arene core and two linking groups appended on four sides, exhibiting a wide range of hexagonal columnar phases, has been synthesised and well characterised. The liquid crystal beha
Anticancer, antimicrobial activities of quinoline based hydrazone analogues: Synthesis, characterization and molecular docking
Katariya, Kanubhai D,Shah, Shailesh R.,Reddy, Dushyanth
supporting information, (2019/11/26)
Based on the biologically active heterocycle quinoline, a series (18a-p) of quinoline hydrazone analogues were prepared, starting from 6-bromo/6-chloro-2-methyl-quinolin-4-yl-hydrazines. For all the newly synthesized compounds cytotoxic activities were carried out at the National Cancer Institute (NCI), USA, against full NCI 60 human cancer cell lines. Amongst all the tested compounds, nine compounds (18b, 18d, 18e, 18f, 18g, 18h, 18i, 18j, 18l) exhibited important anti-proliferative activity at 10 μM concentration and were further screened at 10-fold dilutions of five different concentrations (0.01, 0.1, 1, 10 and 100 μM) with GI50 values ranging from 0.33 to 4.87 μM and LC50 values ranging from 4.67 μM to >100j μM. Further, the mean values of GI50, TGI and LC50 of the most potent compound 18j were compared with the clinically used anticancer agents bendamustine and chlorambucil, revealed that the quinolyl hydrazones holds promise as a potential anticancer agents. Further all the newly prepared compounds were screened for their antimicrobial activity. All the quinolyl hydrazones displayed good to excellent antimicrobial activity with MIC values ranging from 6.25 to 100 μg/mL against the tested pathogenic strains. Molecular docking of the synthesized compounds into the active binding site of human DNA topoisomerase I (htopoI) was carried out to predict the binding mode to the DNA topoisomerase I inhibitors. Hopefully in future, compounds based on quinoline core could be used as a lead compounds for designing new anticancer agents.
Fabrication of deoxycholic acid tethered α-cyanostilbenes as smart low molecular weight gelators and AIEE probes for bio-imaging
Agarwal, Devesh S.,Jha, Prabhat N.,Prakash Singh, Rajnish,Sakhuja, Rajeev
, (2020/05/28)
Four novel deoxycholic acid tethered α-cyanostilbenes were designed, synthesized and characterized using detailed spectroscopic analysis. The synthesized deoxycholic acid tethered α-cyanostilbene derivatives formed stable gels with a variety of solvents,
Effect of regioisomerism on the self-assembly, photophysical and gelation behavior of aroylhydrazone based polycatenars: Synthesis and characterization
Kanth, Priyanka,Singh, Hemant Kumar,Kumar, Vijay,Singh, Sachin Kumar,Rao, D.S. Shankar,Prasad, S. Krishna,Singh, Bachcha
, (2019/07/02)
In this paper we report five series of aroylhydrazone based polycatenars differing from each other in number and position of alkoxy chains on one end of the core; keeping other end the same. A systematic variation in the structures was carried out to understand the effect of position and chain length on the mesophase behavior. In the case of single alkoxy chain at 4-position, there is a transition from Smectic C to Smectic A mesophase during cooling and Smectic A to Smectic C transition in heating cycle in all the homologues except n = 6 & n = 8. In the case of two alkoxy chains at 3-, 5-positions, the compounds are non-mesogenic in nature. On changing the position of alkoxy chains from 3-, 5-positions to 3-, 4-positions, intermolecular forces weaken and these compounds become liquid crystalline and show columnar rectangular mesophase resulting from the effect of regioisomerism. Moving on to the series with three alkoxy chains, it was observed that 2-, 3-, 4-trialkoxy substituted compounds exhibit columnar rectangular mesophase except lower chain length (n = 6 & 8) while 3-, 4-, 5-trialkoxy substituted aroylhydrazones show columnar rectangular mesophase; except n = 10 which shows columnar oblique mesophase. Thus it was established that on increasing density of alkoxy chains around one terminal, mesophase changes from smectic to columnar mesophase. Temperature dependent Raman studies confirm the presence of intermolecular hydrogen bonding. Further, effect of substitution pattern did not show much influence on the photophysical properties of the mesogenic series in solid and solution state. However, the non-mesogenic series showed a different absorption and emission transition from the mesogenic series in solid and solution state. Solid state fluorescence studies show almost similar emission maxima in all the series. However, it was also noticed that non-mesogenic series show maximum red shifted emission maxima in solid state as compared to that of solution. All the series showed good gelation properties with less than 1% CGC (wt%) suggesting the strong ability of molecules to form gel. These H-bonded liquid-crystalline gels have immense potential for applications in emissive displays.
Anhydrous proton conduction in self-assembled and disassembled ionic molecules
Kumar, Avneesh,Pisula, Wojciech,Sieber, Christoph,Klapper, Markus,Müllen, Klaus
, p. 6074 - 6084 (2018/04/12)
In polymer based ionic conductors, the conductivity is suppressed by a low degree of chain mobility, therefore it is imperative to design a molecular system in which ionic groups can be mobilized and immobilized as a function of temperature to allow ions
