Browse
Submit Data
Databases
API
Help

Dataset Information

9 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Immobilization of an Iridium Pincer Complex in a Microporous Polymer for Application in Room-Temperature Gas Phase Catalysis.

ABSTRACT: An iridium dihydride pincer complex [IrH₂ (POCOP)] is immobilized in a hydroxy-functionalized microporous polymer network using the concepts of surface organometallic chemistry. The introduction of this novel, truly innocent support with remote OH-groups enables the formation of isolated active metal sites embedded in a chemically robust and highly inert environment. The catalyst maintained high porosity and without prior activation exhibited efficacy in the gas phase hydrogenation of ethene and propene at room temperature and low pressure. The catalyst can be recycled for at least four times.

SUBMITTER: Konig M

PROVIDER: S-EPMC7692909 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Immobilization of an Iridium Pincer Complex in a Microporous Polymer for Application in Room-Temperature Gas Phase Catalysis.

König Michaela M Rigo Massimo M Chaoui Nicolas N Tran Ngoc Trung T Epping Jan Dirk JD Schmidt Johannes J Pachfule Pradip P Ye Meng-Yang MY Trunk Matthias M Teichert Johannes F JF Drieß Matthias M Thomas Arne A

Angewandte Chemie (International ed. in English) 20200831 45

An iridium dihydride pincer complex [IrH<sub>2</sub> (POCOP)] is immobilized in a hydroxy-functionalized microporous polymer network using the concepts of surface organometallic chemistry. The introduction of this novel, truly innocent support with remote OH-groups enables the formation of isolated active metal sites embedded in a chemically robust and highly inert environment. The catalyst maintained high porosity and without prior activation exhibited efficacy in the gas phase hydrogenation of ...[more]

PMID: 32614513

Similar Datasets

Temperature and Pressure Dependence of Gas Permeation in a Microporous Troger's Base Polymer.

Project description:Gas transport properties of PIM-EA(H?)-TB, a microporous Tröger's base polymer, were systematically studied over a range of pressure and temperature. Permeability coefficients of pure CO?, N?, CH? and H? were determined for upstream pressures up to 20 bar and temperatures up to 200 °C. PIM-EA(H?)-TB exhibited high permeability coefficients in absence of plasticization phenomena. The permeability coefficient of N?, CH? and H? increased with increasing temperature while CO2 permeability decreased with increasing temperature as expected for a glassy polymer. The diffusion and solubility coefficients were also analysed individually and compared with other polymers of intrinsic microporosity. From these results, the activation energies of permeation, diffusion and sorption enthalpies were calculated using an Arrhenius equation.

| S-EPMC6316465 | biostudies-literature

Fabrication of a conjugated microporous polymer membrane and its application for membrane catalysis.

Project description:A flexible and free standing conjugated microporous polymer (CMP) membrane was prepared using a polyvinylpyrrolidone (PVP) electrospun membrane as a template. The PVP nanofibers of the template membrane were coated with a thin layer of the CMP through the in situ Sonogashira-Hagihara coupling reaction of 1,3,5-triethynylbenzene and 1,4-diiodobenzene. The PVP nanofibers were removed by the solvent extraction to produce the CMP membrane, which retained the entangled fibrous structure of the template membrane. Each fiber showed a hollow tubular structure having a CMP wall with a thickness of tens of nanometers. The microporous polymer membrane exhibited a high BET surface area with hierarchical porosity and good permeability. As a catalytic CMP membrane, the Ag nanoparticle-immobilized microporous polymer membrane was fabricated using an electrospun PVP@Ag membrane as a template. After being coated with the CMP, the PVP nanofibers were removed by the solvent extraction, but the Ag nanoparticles were trapped in the microporous polymer shell. The catalytic CMP membrane was successfully used for the catalytic reduction reaction of 4-nitrophenol. The hollow tubular structure and hierarchical porosity of the membrane allowed for the reactants to easily penetrate into the CMP wall and to contact the Ag nanoparticles, resulting in the high catalytic activity.

| S-EPMC5648826 | biostudies-other

Incompatibility of Pure SnO2 Thin Films for Room-Temperature Gas Sensing Application

Project description: Not available

| S-EPMC10500894 | biostudies-literature

Highly sensitive gas-phase explosive detection by luminescent microporous polymer networks.

Project description:We propose microporous networks (MPNs) of a light emitting spiro-carbazole based polymer (PSpCz) as luminescent sensor for nitro-aromatic compounds. The MPNs used in this study can be easily synthesized on arbitrarily sized/shaped substrates by simple and low-cost electrochemical deposition. The resulting MPN afford an extremely high specific surface area of 1300?m(2)/g, more than three orders of magnitude higher than that of the thin films of the respective monomer. We demonstrate, that the luminescence of PSpCz is selectively quenched by nitro-aromatic analytes, e.g. nitrobenzene, 2,4-DNT and TNT. In striking contrast to a control sample based on non-porous spiro-carbazole, which does not show any luminescence quenching upon exposure to TNT at levels of 3?ppm and below, the microporous PSpCz shows a clearly detectable response even at TNT concentrations as low as 5?ppb, clearly demonstrating the advantage of microporous films as luminescent sensors for traces of explosive analytes. This level states the vapor pressure of TNT at room temperature.

| S-EPMC4931441 | biostudies-literature

Hairy Conjugated Microporous Polymer Nanoparticles Facilitate Heterogeneous Photoredox Catalysis with Solvent-Specific Dispersibility.

Project description:Substrate accessibility is a key limiting factor for the efficiency of heterogeneous photoredox catalysis. Recently, a high photoactive surface area of conjugated microporous polymer nanoparticles (CMP NPs) has made them promising candidates for overcoming the mass transfer limitation to achieve high photocatalytic efficiency. However, this potential has not been realized due to limited dispersibility of CMP NPs in many solvents, particularly in water. Here, we report a polymer grafting strategy that furnishes versatile hairy CMP NPs with enhanced solvent-specific dispersibility. The method associates hundreds of solvent-miscible repeating units with one chain end of the photocatalyst surface, allowing minimal modification to the CMP network that preserves its photocatalytic activity. Therefore, the enhanced dispersibility of hairy CMP NPs in organic solvents or aqueous solutions affords high efficiency in various photocatalytic organic transformations.

| S-EPMC9620398 | biostudies-literature

Gas sensing properties of nanocrystalline diamond at room temperature.

Project description:This study describes an integrated NH3 sensor based on a hydrogenated nanocrystalline diamond (NCD)-sensitive layer coated on an interdigitated electrode structure. The gas sensing properties of the sensor structure were examined using a reducing gas (NH3) at room temperature and were found to be dependent on the electrode arrangement. A pronounced response of the sensor, which was comprised of dense electrode arrays (of 50 µm separation distance), was observed. The sensor functionality was explained by the surface transfer doping effect. Moreover, the three-dimensional model of the current density distribution of the hydrogenated NCD describes the transient flow of electrons between interdigitated electrodes and the hydrogenated NCD surface, that is, the formation of a closed current loop.

| S-EPMC4273209 | biostudies-literature

Decarbonylative ether dissection by iridium pincer complexes.

Project description:A unique chain-rupturing transformation that converts an ether functionality into two hydrocarbyl units and carbon monoxide is reported, mediated by iridium(i) complexes supported by aminophenylphosphinite (NCOP) pincer ligands. The decarbonylation, which involves the cleavage of one C-C bond, one C-O bond, and two C-H bonds, along with formation of two new C-H bonds, was serendipitously discovered upon dehydrochlorination of an iridium(iii) complex containing an aza-18-crown-6 ether macrocycle. Intramolecular cleavage of macrocyclic and acyclic ethers was also found in analogous complexes featuring aza-15-crown-5 ether or bis(2-methoxyethyl)amino groups. Intermolecular decarbonylation of cyclic and linear ethers was observed when diethylaminophenylphosphinite iridium(i) dinitrogen or norbornene complexes were employed. Mechanistic studies reveal the nature of key intermediates along a pathway involving initial iridium(i)-mediated double C-H bond activation.

| S-EPMC8162749 | biostudies-literature

Gas Sensing Properties of Perovskite Decorated Graphene at Room Temperature.

Project description:This paper explores the gas sensing properties of graphene nanolayers decorated with lead halide perovskite (CH3NH3PbBr3) nanocrystals to detect toxic gases such as ammonia (NH3) and nitrogen dioxide (NO2). A chemical-sensitive semiconductor film based on graphene has been achieved, being decorated with CH3NH3PbBr3 perovskite (MAPbBr3) nanocrystals (NCs) synthesized, and characterized by several techniques, such as field emission scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. Reversible responses were obtained towards NO2 and NH3 at room temperature, demonstrating an enhanced sensitivity when the graphene is decorated by MAPbBr3 NCs. Furthermore, the effect of ambient moisture was extensively studied, showing that the use of perovskite NCs in gas sensors can become a promising alternative to other gas sensitive materials, due to the protective character of graphene, resulting from its high hydrophobicity. Besides, a gas sensing mechanism is proposed to understand the effects of MAPbBr3 sensing properties.

| S-EPMC6832145 | biostudies-literature

A metal-organic framework immobilised iridium pincer complex.

Project description:An iridium pincer complex has been immobilised in the metal-organic framework NU-1000 using a technique called solvent assisted ligand-incorporation (SALI). The framework proved to be stable under the conditions required to activate the iridium complex and spectroscopic investigations showed formation of the catalytically active iridium dihydride. The Ir-pincer modified NU-1000 is an active catalyst for the condensed phase hydrogenation of a liquid alkene (1-decene and styrene) and shows enhanced activity with respect to a homogeneous analogue. Additionally, the Ir-pincer immobilised inside NU-1000 operated as an efficient heterogenous catalyst under flow conditions.

| S-EPMC6018438 | biostudies-literature

Solid-State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization.

Project description:The use of solid-state molecular organometallic chemistry (SMOM-chem) to promote the efficient double bond isomerization of 1-butene to 2-butenes under flow-reactor conditions is reported. Single crystalline catalysts based upon the ?-alkane complexes [Rh(R2PCH2CH2PR2)(?2?2-NBA)][BArF 4] (R = Cy, tBu; NBA = norbornane; ArF = 3,5-(CF3)2C6H3) are prepared by hydrogenation of a norbornadiene precursor. For the tBu-substituted system this results in the loss of long-range order, which can be re-established by addition of 1-butene to the material to form a mixture of [Rh(tBu2PCH2CH2PtBu2)(cis-2-butene)][BArF 4] and [Rh(tBu2PCH2CH2PtBu2)(1-butene)][BArF 4], in an order/disorder/order phase change. Deployment under flow-reactor conditions results in very different on-stream stabilities. With R = Cy rapid deactivation (3 h) to the butadiene complex occurs, [Rh(Cy2PCH2CH2PCy2)(butadiene)][BArF 4], which can be reactivated by simple addition of H2. While the equivalent butadiene complex does not form with R = tBu at 298 K and on-stream conversion is retained up to 90 h, deactivation is suggested to occur via loss of crystallinity of the SMOM catalyst. Both systems operate under the industrially relevant conditions of an isobutene co-feed. cis:trans selectivites for 2-butene are biased in favor of cis for the tBu system and are more leveled for Cy.

| S-EPMC7147255 | 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