Search results for "Intramolecular force"

showing 10 items of 599 documents

The photophysics and photochemistry of cofacial free base and metallated bisporphyrins held together by covalent architectures

2007

Abstract This review focuses on the photophysical properties of bisporphyrin systems held in a face-to-face configuration by covalent bonds via flexible or rigid spacers and metal–metal bonds. The cofacial arrangement induces intramolecular bismacrocycle interactions promoting basic photophysical events such as excitonic interactions and energy and electron transfers. These events are relevant to mimic light harvesting and reactor devices known for photosynthesis in plants, and can be monitored by luminescence and flash photolysis methods.

Exciton010402 general chemistryPhotochemistryporphyrins01 natural sciencesInorganic Chemistry[ CHIM.OTHE ] Chemical Sciences/OtheremissionMaterials ChemistryluminescencePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSphotophysicsexciton010405 organic chemistryChemistryelectron and energy transferFree base0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryphosphorescenceCovalent bondIntramolecular force[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryFlash photolysisfluorescenceLuminescencePhosphorescence[CHIM.OTHE]Chemical Sciences/Other
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Unveiling the Intramolecular Ionic Diels–Alder Reactions within Molecular Electron Density Theory

2021

The intramolecular ionic Diels–Alder (IIDA) reactions of two dieniminiums were studied within the Molecular Electron Density Theory (MEDT) at the ωB97XD/6-311G(d,p) computational level. Topological analysis of the electron localization function (ELF) of dieniminiums showed that their electronic structures can been seen as the sum of those of butadiene and ethaniminium. The superelectrophilic character of dieniminiums accounts for the high intramolecular global electron density transfer taking place from the diene framework to the iminium one at the transition state structures (TSs) of these IIDA reactions, which are classified as the forward electro density flux. The activation enthalpy ass…

Exergonic reaction010405 organic chemistryChemistryintramolecular ionic Diels–Alder reactionsmolecular electron density theorydieniminiumsIntermolecular forceIminiumIonic bondingGeneral Medicine010402 general chemistry01 natural sciencesElectron localization function0104 chemical sciencesGibbs free energyChemistryCrystallographysymbols.namesakeglobal electron density transferIntramolecular forcesuperelectrophilessymbolsSingle bondQD1-999Chemistry
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High Yield Ultrafast Intramolecular Singlet Exciton Fission in a Quinoidal Bithiophene

2015

We report the process of singlet exciton fission with high-yield upon photoexcitation of a quinoidal thiophene molecule. Efficient ultrafast triplet photogeneration and its yield are determined by photoinduced triplet-triplet absorption, flash photolysis triplet lifetime measurements, as well as by femtosecond time-resolved transient absorption and fluorescence methods. These experiments show that optically excited quinoidal bithiophene molecule undergoes ultrafast formation of the triplet-like state with the lifetime ∼57 μs. CASPT2 and RAS-SF calculations have been performed to support the experimental findings. To date, high singlet fission rates have been reported for crystalline and pol…

FissionChemistryQuantum yieldPhotochemistryPhotoexcitationCondensed Matter::Materials ScienceIntramolecular forceExcited stateSinglet fissionUltrafast laser spectroscopyFlash photolysisGeneral Materials SciencePhysics::Chemical PhysicsPhysical and Theoretical ChemistryThe Journal of Physical Chemistry Letters
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Role of the bridge in photoinduced electron transfer in porphyrin-fullerene dyads.

2015

The role of π-conjugated molecular bridges in through-space and through-bond electron transfer is studied by comparing two porphyrin-fullerene donor-acceptor (D-A) dyads. One dyad, ZnP-Ph-C60 (ZnP = zinc porphyrin), incorporates a phenyl bridge between D and A and behaves very similarly to analogous dyads studied previously. The second dyad, ZnP-EDOTV-C60, introduces an additional 3,4-ethylenedioxythienylvinylene (EDOTV) unit into the conjugated bridge, which increases the distance between D and A, but, at the same time, provides increased electronic communication between them. Two essential outcomes that result from the introduction of the EDOTV unit in the bridge are as follows: 1) faster…

FullereneChemistryOrganic ChemistryGeneral ChemistryPhotochemistryExcimerBridge (interpersonal)PorphyrinCatalysisPhotoinduced electron transferElectron transferchemistry.chemical_compoundPhotoinduced charge separationIntramolecular forceChemistry (Weinheim an der Bergstrasse, Germany)
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Two Decades of Progress in the Asymmetric Intramolecular aza-Michael Reaction.

2021

The asymmetric intramolecular aza-Michael reaction (IMAMR) is a very convenient strategy for the generation of heterocycles bearing nitrogen-substituted stereocenters. Due to the ubiquitous presence of these skeletons in natural products, the IMAMR has found widespread applications in the total synthesis of alkaloids and biologically relevant compounds. The development of asymmetric versions of the IMAMR are quite recent, most of them reported in this century. The fundamental advances in this field involve the use of organocatalysts. Chiral imidazolidinones, diaryl prolinol derivatives, Cinchone-derived primary amines and quaternary ammonium salts, and BINOL-derived phosphoric acids account…

General Chemical EngineeringEnantioselective synthesisTotal synthesisStereoisomerismGeneral ChemistryBiochemistryCombinatorial chemistryStereocenterProlinolchemistry.chemical_compoundAlkaloidschemistryNucleophileIntramolecular forceOrganocatalysisMaterials ChemistryMichael reactionIminesAminesChemical record (New York, N.Y.)
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Synthesis, X-ray Structure, Conformational Analysis, and DFT Studies of a Giant s-Triazine bis-Schiff Base

2021

The current work involves the synthesis of 2,2′-(6-(piperidin-1-yl)-1,3,5-triazine-2,4-diyl)bis(hydrazin-2-yl-1-ylidene))bis(methanylylidene))diphenol 4, characterization, and the DFT studies of the reported compound. The crystal unit cell parameters of 4 are a = 8.1139(2) Å, b = 11.2637(2) Å, c = 45.7836(8) Å. The unit cell volume is 4184.28(15) Å3 and Z = 4. It crystallized in the orthorhombic crystal system and Pbca space group. The O…H, N…H, C…H, H…H and C…C intermolecular contacts which affect the crystal stability were quantitatively analyzed using Hirshfeld calculations. Their percentages were calculated to be 9.8, 15.8, 23.7, 46.4, and 1.6% from the whole contacts occurred in the cr…

General Chemical EngineeringInorganic ChemistryCrystalchemistry.chemical_compounds-triazineNBOGeneral Materials Sciencebis-Schiff basetyppiyhdisteetheterosykliset yhdisteetConformational isomerismkemiallinen synteesiSchiff baseCrystallography<i>s</i>-triazineChemistryHydrogen bondtiheysfunktionaaliteoriaIntermolecular forceconformational analysisHirshfeld analysiskiteetCondensed Matter Physics<i>bis</i>-Schiff baseCrystallographyQD901-999Intramolecular forceOrthorhombic crystal systemröntgenkristallografiaNatural bond orbitalCrystals
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Synthesis and X-ray Crystal Structure of New Substituted 3-4′-Bipyrazole Derivatives. Hirshfeld Analysis, DFT and NBO Studies

2021

A new compounds named 3-4′-bipyrazoles 2 and 3 were synthesized in high chemical yield from a reaction of pyran-2,4-diketone 1 with aryl hydrazines under thermal conditions in MeOH. Compound 2 was unambiguously confirmed by single-crystal X-ray analysis. It crystalizes in a triclinic crystal system and space group P-1. Its crystal structure was found to be in good agreement with the spectral characterizations. With the aid of Hirshfeld calculations, the H…H (54.8–55.3%) and H…C (28.3–29.2%) intermolecular contacts are the most dominant, while the O…H (5.8–6.5%), N…H (3.8–4.6%) and C…C (3.0–4.9%) are less dominant. The compound has a polar nature with a net dipole moment of 6.388 Debye. The …

General Chemical Engineeringpyran-24-dioneCrystal structureTriclinic crystal systemDFTInorganic Chemistrychemistry.chemical_compoundkemialliset sidoksetNBOGeneral Materials Scienceorgaaniset yhdisteetkemiallinen synteesiCrystallographyArylIntermolecular forcetiheysfunktionaaliteoriaHirshfeld analysisCondensed Matter PhysicskiteetbipyrazoleDipoleCrystallographychemistryQD901-999Intramolecular forceYield (chemistry)röntgenkristallografiaNatural bond orbitalCrystals
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π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon

2019

A π-extended double [7]carbohelicene 2 with fused pyrene units was synthesized, revealing considerable intra- and intermolecular π–π interactions as confirmed with X-ray crystallography. As compared to the previous double [7]carbohelicene 1, the π-extended homologue 2 demonstrated considerably red-shifted absorption with an onset at 645 nm (1: 550 nm) corresponding to a smaller optical gap of 1.90 eV (1: 2.25 eV). A broad near-infrared emission from 600 to 900 nm with a large Stokes shift of ∼100 nm (2.3 × 103 cm–1) was recorded for 2, implying formation of an intramolecular excimer upon excitation, which was corroborated with femtosecond transient absorption spectroscopy. Moreover, 2 revea…

General Chemistry010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesChiral column chromatographysymbols.namesakeCrystallographychemistry.chemical_compoundColloid and Surface ChemistrychemistryStokes shiftIntramolecular forceUltrafast laser spectroscopysymbolsPyreneDensity functional theorySpectroscopyIsomerizationJournal of the American Chemical Society
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Definition of the halogen bond (IUPAC Recommendations 2013)

2013

This recommendation proposes a definition for the term “halogen bond”, which designates a specific subset of the inter- and intramolecular interactions involving a halogen atom in a molecular entity.

Halogen bondComputational chemistryChemistryGeneral Chemical EngineeringIntramolecular forceChemical nomenclatureSupramolecular chemistryAtom (order theory)Organic chemistryGeneral ChemistryMolecular entityPure and Applied Chemistry
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Modulation of N···I and +N−H···Cl−···I Halogen Bonding: Folding, Inclusion, and Self-Assembly of Tri- and Tetraamino Piperazine Cyclophanes

2010

The acidity of the crystallization conditions was successfully employed in modulating the balance between the robust intramolecular hydrogen bonding (HB) and intermolecular halogen bonding (XB) observed in large tri- (1) and tetraamino (2) piperazine cyclophanes. A careful crystallization of the title XB acceptor cyclophanes with a strong bidentate XB donor 1,4-diiodotetrafluorobenzene (F4DIB) from CHCl3:MeOH, dimethylformamide (DMF), or HCl:H2O:EtOH resulted in X-ray quality crystals of 1·F4DIB, 2@DMF, 2·2@F4DIB, [1H3]Cl3·(F4DIB)6, and [2H6]Cl6·(F4DIB)2. The intramolecular hydrogen bonding pattern in 1 and 2 was retained in neutral protic and aprotic solvents, and regular N−H···N hydrogen …

Halogen bondStereochemistryHydrogen bondSynthonProtonationGeneral ChemistryCondensed Matter PhysicsMedicinal chemistrychemistry.chemical_compoundPiperazinechemistryIntramolecular forceDimethylformamideGeneral Materials ScienceCyclophaneCrystal Growth &amp; Design
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