Search results for "GRO"

showing 10 items of 31405 documents

High-resolution rovibrational spectroscopy of c-C3H2+: The ν7 C–H antisymmetric stretching band

2020

Abstract The ν 7 antisymmetric C–H stretching fundamental of c- C 3 H 2 + has been characterized in a cryogenic 22-pole ion trap by a novel type of action spectroscopy, in which the rovibrational excitation of c- C 3 H 2 + is detected as a slowing down of the low-temperature reaction c- C 3 H 2 +  + H2 → C 3 H 3 + + H. Ninety-one rovibrational transitions with partly resolved fine structure doublets were measured in high resolution. Supported by high-level quantum chemical calculations, spectroscopic parameters were determined by fitting the observed lines with an effective Hamiltonian for an asymmetric rotor in a doublet electronic ground state, X ˜ A 1 2 , yielding a band origin at 3113.6…

010405 organic chemistryAntisymmetric relationChemistryOrganic ChemistryRotational–vibrational spectroscopy010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciencesAnalytical ChemistryInorganic Chemistrysymbols.namesakesymbolsMoleculeIon trapGround stateHamiltonian (quantum mechanics)SpectroscopySpectroscopyExcitationJournal of Molecular Structure
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Tuning the Electronic Properties of Nonplanar exTTF-Based Push–Pull Chromophores by Aryl Substitution

2012

International audience; A new family ofπ-extended tetrathiafulvalene (exTTF) donor−acceptorchromophores has been synthesized by [2 + 2] cycloaddition of TCNE with exTTF-substituted alkynes and subsequent cycloreversion. X-ray data and theoretical calculations,performed at the B3LYP/6-31G**level, show that the new chromophores exhibit highlydistorted nonplanar molecular structures with largely twisted 1,1,4,4-tetracyanobuta-1,3-diene (TCBD) units. The electronic and optical properties, investigated by UV/visspectroscopy and electrochemical measurements, are significantly modified when theTCBD acceptor unit is substituted with a donor phenyl group, which increases the twistingof the TCBD unit…

010405 organic chemistryBand gap[CHIM.ORGA]Chemical Sciences/Organic chemistryArylOrganic ChemistryChromophore010402 general chemistryPhotochemistry01 natural sciencesAcceptorCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPhenyl groupSpectroscopyTetrathiafulvaleneComputingMilieux_MISCELLANEOUS
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Computational study of the spin-forbidden H 2 oxidative addition to 16-electron Fe(0) complexes

2003

International audience; The spin-forbidden oxidative addition of H2 to Fe(CO)4, Fe(PH3)4, Fe(dpe)2 and Fe(dmpe)2 [dpe = H2PCH2CH2PH2, dmpe = (CH3)2PCH2CH2P(CH3)2] has been investigated by density functional theory using a modified B3PW91 functional. All 16-electron fragments are found to adopt a spin triplet ground state. The H2 addition involves a spin crossover in the reagents region of configurational space, at a significantly higher energy relative to the triplet dissociation asymptote and, for the case of Fe(CO)4·H2, even higher than the singlet dissociation asymptote. After crossing to the singlet surface, the addition proceeds directly to the classical cis-dihydride product. Only for…

010405 organic chemistryChemistry010402 general chemistryPhotochemistry01 natural sciencesOxidative additionDissociation (chemistry)0104 chemical sciencesInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrySpin crossoverMoleculePhysical chemistryDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet stateDihydrogen complexGround state
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Assembling Halogen-Bonded Capsules via Cation Exchange

2017

Dr. Lotta Turunen is currently a postdoctoral researcher within Acad. Prof. Kari Rissanen's research group at the University of Jyvaskyla in Finland. Under his supervision, she obtained her MSc in organic chemistry and completed her PhD in chemistry in late September 2017. Her research focused on designing, synthesizing, and characterizing halogen-bonded supramolecular assemblies, capsules, and cages.

010405 organic chemistryChemistryGeneral Chemical EngineeringBiochemistry (medical)Supramolecular chemistryNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesGroup (periodic table)HalogenMaterials ChemistryEnvironmental ChemistryOrganic chemistryChem
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Ring opening polymerization of d,l-lactide and ε-caprolactone catalysed by (pyrazol-1-yl)copper(ii) carboxylate complexes

2021

1,2-Bis{(3,5-dimethylpyrazol-1-yl)methyl}benzene (L) reacts with [Cu(OAc)2] and C6H5COOH, 4-OH-C6H4COOH, 2-Cl-C6H4COOH and (3,5-NO2)2-C6H3COOH to afford the copper complexes [Cu2(C6H5COO)4(L)2] (1), [Cu2(4-OH-C6H4COO)4(L)2] (2), [Cu2(2-Cl-C6H4COO)4(L)2]n (3) and [Cu{(3,5-NO2)2-C6H3COO}2L]n (4) which are characterised by IR, mass spectrometry, elemental analyses, and X-ray crystallography. The structural data revealed two geometries that are adopted by the complexes: (i) paddle wheel in 1, 2·7H2O, 3 and (ii) regular chains in 3 and 4. Magnetic studies show strong antiferromagnetic couplings in the paddle wheel complexes and a weak antiferromagnetic coupling in the monometallic chain one. Cat…

010405 organic chemistryChemistryGeneral Chemical EngineeringDispersityGeneral Chemistry010402 general chemistry01 natural sciencesRing-opening polymerization0104 chemical scienceschemistry.chemical_compoundEnd-groupPaddle wheelPolymerizationPolycaprolactonePolymer chemistryCarboxylateCaprolactoneRSC Advances
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Mechanism of activated chemiluminescence of cyclic peroxides: 1,2-dioxetanes and 1,2-dioxetanones

2017

Almost all chemiluminescent and bioluminescent reactions involve cyclic peroxides. The structure of the peroxide and reaction conditions determine the quantum efficiency of light emission. Oxidizable fluorophores, the so-called activators, react with 1,2-dioxetanones promoting the former to their first singlet excited state. This transformation is inefficient and does not occur with 1,2-dioxetanes; however, they have been used as models for the efficient firefly bioluminescence. In this work, we use the SA-CASSCF/CASPT2 method to investigate the activated chemiexcitation of the parent 1,2-dioxetane and 1,2-dioxetanone. Our findings suggest that ground state decomposition of the peroxide com…

010405 organic chemistryChemistryGeneral Physics and Astronomy010402 general chemistryPhotochemistrySupermolecule01 natural sciencesPeroxideLUCIFERIDAE0104 chemical scienceslaw.inventionchemistry.chemical_compoundlawExcited stateBioluminescenceLight emissionSinglet statePhysical and Theoretical ChemistryGround stateChemiluminescencePhysical Chemistry Chemical Physics
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Intermolecular and Intramolecular Transamidation Reactions

2006

The amide functional group is resonance stabilised and direct reaction with amines is known to be difficult. Facile amide exchange reactions would enable the synthesis of important new amide based molecules, therefore transamidation reactions represent an important step in this direction. In order to ensure a transamidation reaction takes place, special requirements and conditions are required. According to the different structural characteristics of the carbox-amide group and types of activation, the most relevant examples of this reaction will be reviewed.

010405 organic chemistryChemistryIntermolecular forceGeneral MedicinePhotochemistry010402 general chemistryResonance (chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundComputational chemistryIntramolecular forceAmideFunctional groupPolymer chemistryDirect reactionPhysical and Theoretical ChemistryProgress in Reaction Kinetics and Mechanism
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A trigonal prismatic anionic iron(iii) complex of a radical o-iminobenzosemiquinonate derivative: structural and spectral analyses

2017

A new iron(III) complex, [Et3NH][FeIII(L2−˙)2] (1) with a substituted o-aminophenol based ligand is reported. Complex 1 is an anionic complex with a triethylammonium cation in the lattice. It contains two O,O,N-coordinated o-iminobenzosemiquinonate(2−) radical anions with an Fe(III) centre in a high-spin configuration. The crystal structure of 1 was determined by X-ray diffraction, which revealed a trigonal prismatic coordination environment whose electronic structure was established by various physical methods including EPR, Mossbauer spectroscopy and variable-temperature (2–300 K) magnetic susceptibility measurements. Electrochemical analysis indicated primarily ligand-centred redox proce…

010405 organic chemistryChemistryLigandGeneral ChemistryCrystal structureElectronic structure010402 general chemistryTrigonal prismatic molecular geometry01 natural sciencesMagnetic susceptibilityCatalysis0104 chemical scienceslaw.inventionCrystallographylawMössbauer spectroscopyMaterials ChemistryGround stateElectron paramagnetic resonanceNew Journal of Chemistry
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NMR T1-Relaxation Measurements on Paramagnetic Organolanthanides: An Alternative Tool for Structure Determination in Solution

2005

1H NMR investigations were conducted on four paramagnetic organolanthanides, all bearing the tetraisopropylcyclopentadienyl ligand Cp4i (HC5iPr4) in order to verify whether or not interactions observed in the solid state are maintained in solution. In some cases variable-temperature experiments were necessary to enhance the resolution and determine the best conditions for the study. The 1D NMR spectrum could be interpreted in every case. Complementary 2D COSY experiments allowed the full attribution of the signals. T1 (1H) relaxation values were determined for all the paramagnetic complexes at the most suitable temperature, and compared with those of the diamagnetic KCp4i. The same tendency…

010405 organic chemistryChemistryLigandRelaxation (NMR)Analytical chemistrySpin–lattice relaxation[ CHIM.COOR ] Chemical Sciences/Coordination chemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesParamagnetic complexesInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographyNMR spectroscopyOxidation stateLanthanidesProton NMR[CHIM.COOR]Chemical Sciences/Coordination chemistryMethyl groupSpin-lattice relaxation times
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A Fully Conjugated TTF-π-TCAQ System: Synthesis, Structure, and Electronic Properties

2011

The synthesis of the first fully conjugated tetrathiafulvalene-tetracyano-p-quinodimethane ((TTF)-TCNQ)-type system has been carried out by means of a Julia-Kocienski olefination reaction. In particular, a tetracyanoanthraquinodimethane (TCAQ) formyl derivative and two new sulfonylmethyl-exTTFs (exTTF = 2-[9-(1,3-dithiol-2-ylidene)anthracen-10(9H)-ylidene]-1,3-dithiole)--prepared as new building blocks--were linked. A variety of experimental conditions reveal that the use of sodium hexamethyldisilazane (NaHMDS) as base in THF afforded the E olefins with excellent stereoselectivity. Theoretical calculations at the B3LYP/6-31G** level point to highly distorted exTTF and TCAQ that form an almo…

010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryConjugated system010402 general chemistryPhotochemistry01 natural sciencesAcceptorCatalysis0104 chemical sciencesIonchemistry.chemical_compoundRadical ionExcited stateGround stateDerivative (chemistry)TetrathiafulvaleneChemistry - A European Journal
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