Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Iodine and Nickel Ions Adsorption by Conjugated Copolymers Bearing Repeating Units of Dicyclopentapyrenyl and Various Thiophene Derivatives.

ABSTRACT: The synthesis of three conjugated copolymers TPP1-3 was carried out using a palladium-catalyzed [3+2] cycloaddition polymerization of 1,6-dibromopyrene with various dialkynyl thiophene derivatives 3a-c. The target copolymers were obtained in excellent yields and high purity, as confirmed by instrumental analyses. TPP1-3 were found to divulge a conspicuous iodine adsorption capacity up to 3900 mg g^-1, whereas the adsorption mechanism studies revealed a pseudo-second-order kinetic model. Furthermore, recyclability tests of TPP3, the copolymer which revealed the maximum iodine uptake, disclosed its efficient regeneration even after numerous adsorption-desorption cycles. Interestingly, the target copolymers proved promising nickel ions capture efficiencies from water with a maximum equilibrium adsorption capacity (q_e) of 48.5 mg g^-1.

SUBMITTER: Shetty S

PROVIDER: S-EPMC10611155 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Iodine and Nickel Ions Adsorption by Conjugated Copolymers Bearing Repeating Units of Dicyclopentapyrenyl and Various Thiophene Derivatives.

Shetty Suchetha S Baig Noorullah N Wahed Sk Abdul SA Hassan Atikur A Das Neeladri N Alameddine Bassam B

Polymers 20231019 20

The synthesis of three conjugated copolymers TPP1-3 was carried out using a palladium-catalyzed [3+2] cycloaddition polymerization of 1,6-dibromopyrene with various dialkynyl thiophene derivatives 3a-c. The target copolymers were obtained in excellent yields and high purity, as confirmed by instrumental analyses. TPP1-3 were found to divulge a conspicuous iodine adsorption capacity up to 3900 mg g<sup>-1</sup>, whereas the adsorption mechanism studies revealed a pseudo-second-order kinetic model ...[more]

PMID: 37896396

Similar Datasets

Efficient Iodine Uptake of Ultra Thermally Stable Conjugated Copolymers Bearing Biaceanthrylenyl Moieties and Contorted Aromatic Units Using a [3 + 2] Palladium-Catalyzed Cyclopolymerization Reaction.

Project description:A novel series of copolymers made from alternating aromatic surrogates with contorted and spiro compounds, denoted as BCP1-3, was successfully synthesized employing a palladium-catalyzed one-pot [3 + 2] cyclopentannulation reaction. The resulting copolymers BCP1-3, which were isolated in high yields, exhibited weight-average molecular weights (Mw) ranging from 11.0 to 61.5 kg mol-1 (kDa) and polydispersity index (Mw/Mn) values in the range of 1.7 and 2.0, which suggest a narrow molecular weight distribution, thus indicating the formation of uniform copolymer chains. Investigation of the thermal properties of BCP1-3 by thermogravimetric analysis disclosed outstanding stability with 10% weight loss temperature values reaching 800 °C. Iodine adsorption tests revealed remarkable results, particularly for BCP2, which demonstrated a strong affinity toward iodine reaching an uptake of 2900 mg g-1. Additionally, recyclability tests showcased the effective regeneration of BCP2 after several successive iodine adsorption-desorption cycles.

| S-EPMC10653061 | biostudies-literature

Fluorinated Iron(ii) clathrochelate units in metalorganic based copolymers: improved porosity, iodine uptake, and dye adsorption properties.

Project description:We report the synthesis of metalorganic copolymers made from the palladium catalyzed Sonogashira cross-coupling reaction between various iron(ii) clathrochelate building blocks with diethynyl-triptycene and fluorene derivatives. The target copolymers CCP1-5 were isolated in excellent yield and characterized by various instrumental analysis techniques. Interestingly, investigation of the copolymers' porosity properties discloses BET surface areas up to 337 m2 g-1 for the target compounds bearing fluorinated iron(ii) clathrochelate units CCP2,5. Moreover, the fluorinated copolymers display an outstanding uptake capacity of iodine with a maximum adsorption of 200 wt%. The target metalorganic copolymers CCP1-5 reveal very good adsorption of organic dyes, namely, methyl blue and methylene blue, from aqueous media.

| S-EPMC8697800 | biostudies-literature

Design and Characterization of New D-A Type Electrochromic Conjugated Copolymers Based on Indolo[3,2-b]Carbazole, Isoindigo and Thiophene Units.

Project description:Two new donor-acceptor (D-A) type organic conjugated random copolymers were successfully synthesized by three-component Stille coupling polymerization of indolo[3,2-b]carbazole (ICZ), isoindigo (IID) and thiophene units, namely PITID-X (X = 1 and 2), with the controlled monomer feed ratios of 3:1:4 and 1:1:2, respectively. The strategy of incorporating different alkyl-branched donor/acceptor units and raw material feed ratios facilitated the improvement of optical properties, solubility, conjugated structure, and electrochromic performance. Cyclic voltammetry, UV-vis-NIR absorption spectra, kinetic and colorimetric measurements of the spray-coated films were recorded in the fabricated three-electrode cells. The results showed that PITID-2, whose optical/electrical properties were better than that of PITID-1, was the candidate electrochromic material due to low band gap of 1.58 eV accompanying the color changing from cyan (neutral state) to gray (oxidized state). The copolymer also illustrated fast bleaching/coloration response time of 2.04/0.33 and 1.35/1.50 s in a 4 s time interval, high coloration efficiency of 171.52 and 153.08 cm2 C-1 and stable optical contrast of 18% and 58% at the wavelength of 675 and 1600 nm, respectively.

| S-EPMC6836008 | biostudies-literature

Liquid Crystalline π-Conjugated Copolymers Bearing a Pyrimidine Type Mesogenic Group

Project description:Phenylene-thiophene-based liquid crystalline π-conjugated copolymers bearing mesogenic groups as side chains were synthesized via a Stille polycondensation reaction and confirmed to exhibit a nematic liquid crystal phase at appropriate temperatures. The formation of a nematic phase, but not a smectic phase indicates cooperation of the main chain and side chain in the formation of a nematic main-chain/side-chain liquid crystal phase. The generation of polarons in the main chain as charge carriers during in-situ vapor doping of iodine is confirmed to increase with a doping progresses, exhibiting Dysonian paramagnetic behavior typical of conductive polymers.

| S-EPMC5445693 | biostudies-literature

Simple Route to Synthesize Fully Conjugated Ladder Isomer Copolymers with Carbazole Units.

Project description:Two isomer polymers, P3 and P6, with fully conjugated ladder structures are presented by simple synthetic routes. The well-defined structures of fully conjugated ladder polymers P3 and P6 were ensured by the high yields of every reaction step. The fully rigid ladder structures were confirmed by nuclear magnetic resonance (NMR), fourier transform infrared spectroscopy (FTIR), and photophysical test. Polymers P3 and P6 with bulky alkyl side chains exhibit good solution processability and desirable thermostable properties. After the intramolecular cyclization reaction, the band gaps of polymers P3 and P6 become lower (2.86 eV and 2.66 eV, respectively) compared with polymers P1 and P4. This initial study provides insight for the rational design of fully ladder-conjugated isomeric polymers with well-defined structures.

| S-EPMC6835825 | biostudies-literature

New fused conjugated molecules with fused thiophene and pyran units for organic electronic materials.

Project description:Rigid and planar conjugated molecules have substantial significance due to their potential applications in organic electronics. Herein we report two highly fused ladder type conjugated molecules, TTCTTC and TTTCTTTC, with up to 10 fused rings in which the fused-thiophene rings are fused to the chromeno[6,5,4-def]chromene unit. Both molecules show high HOMO levels and accordingly they can be oxidized into their radical cations with absorptions extending to 1300 nm in the presence of trifluoroacetic acid. Thin films of TTCTTC and TTTCTTTC exhibit p-type semiconductor properties with hole mobilities up to 0.39 cm2 V-1 s-1. Moreover, TTCTTC shows a high fluorescence quantum yield of up to 16.5% in the solid state.

| S-EPMC9050829 | biostudies-literature

Constructing "breathing" dynamic skeletons with extra π-conjugated adsorption sites for iodine capture.

Project description:Radioiodine (129I and 131I) emission from the nuclear waste stream has aroused enormous apprehension because of its quick diffusion and radiological contamination. Conventional porous adsorbents such as zeolites and carbon with rigid skeletons and constant pore volumes reveal a limited performance for reliable storage. Here, a series of soft porous aromatic frameworks (PAFs) with additional π-conjugated fragments is disclosed to serve as physicochemical stable media. Due to the flexibility of the tertiary amine center, the PAF products provide sufficient space for the binding sites, and thus exhibit a considerable capability for iodine capture from both gaseous and soluble environments. The obtained capacity of PAFs is ca. 1.6 times higher than that of PAF-1 which possesses similar aromatic constituents featuring an ultra-large specific surface area (BET = 5600 m2 g-1). The novel paradigm of dynamic frameworks is of fundamental importance for designing adsorbents to treat environmental pollution issues.

| S-EPMC9066021 | biostudies-literature

Fluorination Effect for Highly Conjugated Alternating Copolymers Involving Thienylenevinylene-Thiophene-Flanked Benzodithiophene and Benzothiadiazole Subunits in Photovoltaic Application.

Project description:Two two-dimensional (2D) donor-acceptor (D-A) type conjugated polymers (CPs), namely, PBDT-TVT-BT and PBDT-TVT-FBT, in which two ((E)-(4,5-didecylthien-2-yl)vinyl)- 5-thien-2-yl (TVT) side chains were introduced into 4,8-position of benzo[1,2-b:4,5-b']dithiophene (BDT) to synthesize the highly conjugated electron-donating building block BDT-TVT, and benzothiadiazole (BT) and/or 5,6-difluoro-BT as electron-accepting unit, were designed to systematically ascertain the impact of fluorination on thermal stability, optoelectronic property, and photovoltaic performance. Both resultant copolymers exhibited the lower bandgap (1.60 ~ 1.69 eV) and deeper highest occupied molecular orbital energy level (EHOMO, -5.17 ~ -5.37 eV). It was found that the narrowed absorption, deepened EHOMO and weakened aggregation in solid film but had insignificant influence on thermal stability after fluorination in PBDT-TVT-FBT. Accordingly, a PBDT-TVT-FBT-based device yielded 16% increased power conversion efficiency (PCE) from 4.50% to 5.22%, benefited from synergistically elevated VOC, JSC, and FF, which was mainly originated from deepened EHOMO, increased μh, μe, and more balanced μh/μe ratio, higher exciton dissociation probability and improved microstructural morphology of the photoactive layer as a result of incorporating fluorine into the polymer backbone.

| S-EPMC7254375 | biostudies-literature

Donor-acceptor random regioregular π-conjugated copolymers based on poly(3-hexylthiophene) with unsymmetrical monothienoisoindigo units.

Project description:Donor-acceptor π-conjugated random copolymers based on regioregular poly(3-hexylthiophene), rr-P3HT, with unsymmetrical monothienoisoindigo moieties were obtained by direct arylation polycondensation of 2-bromo-3-hexylthiophene with unsymmetrical monothienoisoindigo motifs under the optimized conditions [palladium-immobilized on thiol-modified silica gel with chloride counter anions, PITS-Cl (2.5 mol%), PivOH (1.0 equiv.), K2CO3 (3.0 equiv.), DMAc, 100 °C, 24 h]. Incorporation of unsymmetrical monothienoisoindigo electron-acceptor units into the polymers tuned their highest occupied and lowest unoccupied molecular orbital levels, which were close to those of the hole transport material (PEDOT) and electron transport material (PCBM), respectively, in thin-film organic solar cells. Alkyl chains of the unsymmetrical monothienoisoindigo units in the polymers tuned their macrostructural order, resulting in the observation of crystalline patterns and specific absorption peaks in thin films. An organic solar cell containing the most crystalline random copolymer showed an efficiency of 1.91%.

| S-EPMC9053906 | biostudies-literature

Selective adsorption of Hg(ii) with diatomite-based mesoporous materials functionalized by pyrrole-thiophene copolymers: condition optimization, application and mechanism.

Project description:A novel diatomite-based mesoporous material of MCM-41/co-(PPy-Tp) was prepared with MCM-41 as carrier and functionalized with the copolymer of pyrrole and thiophene. The physicochemical characteristics of the as-prepared materials were characterized by various characterization means. The removal behaviour of Hg(ii) was adequately investigated via series of single factor experiments and some vital influence factors were optimized via response surface methodology method. The results exhibit that diatomite-based materials MCM-41/co-(PPy-Tp) has an optimal adsorption capability of 537.15 mg g-1 towards Hg(ii) at pH = 7.1. The removal process of Hg(ii) onto MCM-41/co-(PPy-Tp) is controlled by monolayer chemisorption based on the fitting results of pseudo-second-order kinetic and Langmuir models. In addition, the adsorption of Hg(ii) ions onto MCM-41/co-(PPy-Tp) is mainly completed through forming a stable complex with N or S atoms in MCM-41/co-(PPy-Tp) by electrostatic attraction and chelation. The as-developed MCM-41/co-(PPy-Tp) displays excellent recyclability and stabilization, has obviously selective adsorption for Hg(ii) in the treatment of actual electroplating wastewater. Diatomite-based mesoporous material functionalized by the copolymer of pyrrole and thiophene exhibits promising application prospect.

| S-EPMC9673902 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data