ABSTRACT
A p-type thermoelectric conjugated polymer based on indacenodithiophene and benzothiadiazole is designed and synthesized by replacing normal aliphatic side chains (P1) with conjugated aromatic benzene substituents (P2). The introduced bulky substituent on P2 is detrimental to form the intensified packing of polymers, therefore, it hinders the efficient transporting of the charge carriers, eventually resulting in a lower conductivity compared to that of the polymers bearing aliphatic side chains (P1). These results reveal that the modification of side chains on conjugated polymers is crucial to rationally designed thermoelectric polymers with high performance.
Subject(s)
Benzene/chemistry , Organic Chemicals/chemistry , Polymers/chemistry , Power PlantsABSTRACT
Three novel organic dyes coded as FHD4-1, FHD4-2, and FHD4-3 featuring spiro[dibenzo[3,4:6,7]cyclohepta[1,2-b]quinoxaline-10,9'-fluorene] (SDBQX) moieties are designed to inhibit dye aggregation to improve the performance of dye-sensitized solar cells (DSSCs). The consistent absorption onsets of FHD4-1, FHD4-2, and FHD4-3 in solutions and adsorbed on TiO2 films indicate that these dyes are aggregation-free dyes. Therefore, coadsorption with chenodeoxycholic acid (CDCA) of these three dyes reduces the performance of DSSCs because no inhibition effect for dye aggregation is needed, but, on the contrary, the dye loading amount is reduced after addition of CDCA.
ABSTRACT
An Fe(II) SCO complex based on an acylhydrazone ligand with an amino functional group has been prepared. The complex is able to dissociate and regather upon protonation and deprotonation, in both solid state and solution, accompanied by spin state switching, marked change of color, and distinct solubility in water. Moreover, the complex shows distinct magnetic responses toward formaldehyde and protic and nonprotic solvents, as a result of the different affinity of the amino functional site with those chemicals.
ABSTRACT
Two 9,10-distyrylanthracene-based luminophores exhibiting aggregation-induced emission and stimuli-responsive properties were synthesized. Seven- or five-color luminescence switching based on a single organic molecule was achieved for the first time. These phase transitions can be induced by physical stimuli such as grinding by mortar and pestle, heating, and exposure to the vapors of organic solvents. Moreover, a strategy for the design of new mechanoresponsive materials with π-conjugated luminophores is proposed.
ABSTRACT
The binding mode analysis of Gefitinib revealed that 6-propylmorpholino group (sidechain) shows no interactions due to its weak electron density. In order to modify the electron density of Gefitinib's sidechain, novel pyrrolidino analogs of Gefitinib where morpholino groups were replaced by substituted pyrrolidino groups were synthesized. Gefitinib derivatives with high electronegativity atoms or groups in the pyrrolidino moiety always exhibit high potent activity against EGFR and human cancer cell lines, A431, MDA-MB-231 and A549. Among these derivatives, 16 displayed the best pharmacokinetic properties that make it to be a promising candidate for developing drugs to replace Gefitinib.
Subject(s)
Antineoplastic Agents/pharmacology , ErbB Receptors/antagonists & inhibitors , Protein Kinase Inhibitors/pharmacology , Pyrrolidines/pharmacology , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/chemistry , Cell Line, Tumor , Cell Proliferation/drug effects , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , ErbB Receptors/metabolism , Humans , Molecular Structure , Protein Kinase Inhibitors/chemical synthesis , Protein Kinase Inhibitors/chemistry , Pyrrolidines/chemical synthesis , Pyrrolidines/chemistry , Structure-Activity RelationshipABSTRACT
Two new mononuclear Fe(II) complexes, [FeL1(NCBH3)2] (1) and [FeL2(CN)2]·3H2O (2) (L1 = N,N'-bis(2-pyridylmethyl)-1,2-ethanediamine, L2 = N-(2-pyridylmethyl)-N'-(2-pyridylmethylene)-1,2-ethanediamine) were synthesized from the same starting solution under different atmospheric conditions. Complex 1 was isolated under an N2 atmosphere with an expected molecular structure, namely a tetradentate L1 ligand and two NCBH3(-) co-ligands wrapping an iron(ii) ion. It exhibits a gradual spin crossover centered around 355 K, as confirmed by X-ray crystallography, magnetic, DSC and Mössbauer studies. Complex 2 was isolated in the presence of air. One of the secondary amine groups in L1 undergoes an in situ oxidative dehydrogenation, forming a new monoimine asymmetric ligand L2. Besides, a CN(-) co-ligand is also in situ generated from NCBH3(-) during the reaction. The strong ligand field strength imposed by CN(-) and L2 stabilizes 2 in the LS state. Solvent water molecules in complex 2 are hydrogen bonded into a well-defined 1D water chain. 2 shows a proton conductivity of 8.9 × 10(-5) S cm(-1) at 55 °C and 95% relative humidity.
