0000000000496995

AUTHOR

Jun Shen

showing 4 related works from this author

Comparison of the subjective satisfaction of the donor site morbidity : free radial forearm flap versus anterolateral thigh flap for reconstruction i…

2018

Background The purpose of the study was to compare the differences of the subjective satisfaction of the donor site morbidity between the free radial forearm flap (FRFF) and anterolateral thigh flap (ALTF) for tongue reconstruction. Material and Methods One hundred and nineteen patients underwent FRFF or ALTF reconstruction were retrospectively evaluated by a standardized self-established donor site morbidity questionnaire which included 5 domains, sensibility, movement disabilities, cosmetics, social activities and general impacts on the quality of life. Results The Cronbach’s coefficient alpha of the questionnaire was 0.707. The exploratory factor analysis revealed that the 5 items of the…

AdultMalemedicine.medical_specialtySurgical Flaps03 medical and health sciencesYoung Adult0302 clinical medicinePatient satisfactionPostoperative ComplicationsQuality of lifeCronbach's alphaTongueTongueSurveys and QuestionnairesmedicineHumansGeneral DentistryAgedRetrospective StudiesRadial forearm flapbusiness.industryResearchCancerReproducibility of ResultsRetrospective cohort study030206 dentistryAnterolateral thighMiddle AgedPlastic Surgery Proceduresmedicine.disease:CIENCIAS MÉDICAS [UNESCO]SurgeryTongue NeoplasmsForearmmedicine.anatomical_structureOtorhinolaryngologyThighPatient SatisfactionUNESCO::CIENCIAS MÉDICASQuality of LifeSurgeryFemaleMorbidityOral Surgerybusiness
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The Ground State Electronic Energy of Benzene.

2020

We report on the findings of a blind challenge devoted to determining the frozen-core, full configuration interaction (FCI) ground state energy of the benzene molecule in a standard correlation-consistent basis set of double-$\zeta$ quality. As a broad international endeavour, our suite of wave function-based correlation methods collectively represents a diverse view of the high-accuracy repertoire offered by modern electronic structure theory. In our assessment, the evaluated high-level methods are all found to qualitatively agree on a final correlation energy, with most methods yielding an estimate of the FCI value around $-863$ m$E_{\text{H}}$. However, we find the root-mean-square devia…

Computer sciencephysics.chem-phFOS: Physical sciencesElectronic structure01 natural sciencesFull configuration interactionQuality (physics)5102 Atomic Molecular and Optical PhysicsAffordable and Clean EnergyPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceStatistical physicsPhysical and Theoretical Chemistry010306 general physicsBasis setChemical Physics (physics.chem-ph)34 Chemical Sciences010304 chemical physics3. Good healthPhysical SciencesChemical Sciences3406 Physical ChemistryBenchmark (computing)7 Affordable and Clean EnergyElectronic energyGround state51 Physical SciencesEnergy (signal processing)
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Design and synthesis of the first triply twisted Möbius annulene.

2014

As long as 50 years ago theoretical calculations predicted that Mobius annulenes with only one π surface and one edge would exhibit peculiar electronic properties and violate the Huckel rules. Numerous synthetic attempts notwithstanding, the first singly twisted Mobius annulene was not prepared until 2003. Here we present a general, rational strategy to synthesize triply or even more highly twisted cyclic π systems. We apply this strategy to the preparation of a triply twisted [24]dehydroannulene, the structure of which was confirmed by X-ray analysis. Our strategy is based on the topological transformation of 'twist' into 'writhe'. The advantage is twofold: the product exhibits a lower deg…

Surface (mathematics)Models MolecularMacrocyclic CompoundsMolecular StructureChemistryGeneral Chemical EngineeringStructure (category theory)Molecular ConformationGeneral ChemistryAnnuleneTopological transformationTheoretical physicsComputational chemistryProduct (mathematics)TwistLower degreeWritheNature chemistry
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CCDC 938919: Experimental Crystal Structure Determination

2014

Related Article: Gaston R. Schaller, Filip Topić, Kari Rissanen, Yoshio Okamoto, Jun Shen, Rainer Herges|2014|Nature Chemistry|6|608|doi:10.1038/NCHEM.1955

Space GroupCrystallography111213142728293043444546-dodecadehydropentanaphtho[1'2':1718;1''2'':910;2'''1''':1516;2''''1'''':2324;2'''''1''''':78]cyclotetracosa[12-a]naphthalene chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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