3,003 research outputs found
Catalytic difunctionalization of unactivated alkenes with unreactive hexamethyldisilane through regeneration of silylium ions
A metalâfree, intermolecular synâaddition of hexamethyldisilane across simple alkenes is reported. The catalytic cycle is initiated and propagated by the transfer of a methyl group from the disilane to a silyliumâionâlike intermediate, corresponding to the (re)generation of the silyliumâion catalyst. The key feature of the reaction sequence is the cleavage of the SiâSi bond in a 1,3âsilyl shift from silicon to carbon. A central intermediate of the catalysis was structurally characterized by Xâray diffraction, and the computed reaction mechanism is fully consistent with the experimental findings.TU Berlin, Open-Access-Mittel - 201
Negotiation-based Choreography of Data-intensive Applications in the C3Grid Project
We present a negotiation and agreement strategy and protocol for the efficient scheduling of data intensive jobs in the Grid. It was developed with the background of the Collaborative Climate Community Data and Processing Grid (C3Grid), which provides a comprehensive infrastructure for solving computational problems in Earth System Science. The presented solution is a subset of the overall C3Grid architecture and especially focuses on the collaboration of Data Management and Workflow Scheduling. We evaluate our approach on a case study representing a complex application typical for climate research. Finally, extensions for future work â especially on standardization efforts â are reviewed
Accurate Treatment of Large Supramolecular Complexes by Double-Hybrid Density Functionals Coupled with Nonlocal van der Waals Corrections
In this work, we present a thorough assessment of the performance of some representative double-hybrid density functionals (revPBE0-DH-NL and B2PLYP-NL) as well as their parent hybrid and GGA counterparts, in combination with the most modern version of the nonlocal (NL) van der Waals correction to describe very large weakly interacting molecular systems dominated by noncovalent interactions. Prior to the assessment, an accurate and homogeneous set of reference interaction energies was computed for the supramolecular complexes constituting the L7 and S12L data sets by using the novel, precise, and efficient DLPNO-CCSD(T) method at the complete basis set limit (CBS). The correction of the basis set superposition error and the inclusion of the deformation energies (for the S12L set) have been crucial for obtaining precise DLPNO-CCSD(T)/CBS interaction energies. Among the density functionals evaluated, the double-hybrid revPBE0-DH-NL and B2PLYP-NL with the three-body dispersion correction provide remarkably accurate association energies very close to the chemical accuracy. Overall, the NL van der Waals approach combined with proper density functionals can be seen as an accurate and affordable computational tool for the modeling of large weakly bonded supramolecular systems.Financial support by the âMinisterio de EconomĂa y Competitividadâ (MINECO) of Spain and European FEDER funds through projects CTQ2011-27253 and CTQ2012-31914 is acknowledged. The support of the Generalitat Valenciana (Prometeo/2012/053) is also acknowledged. J.A. thanks the EU for the FP7-PEOPLE-2012-IEF-329513 grant. J.C. acknowledges the âMinisterio de EducaciĂłn, Cultura y Deporteâ (MECD) of Spain for a predoctoral FPU grant
Performance of ab initio and density functional methods for conformational equilibria of CnH2n+2 alkane isomers (n=2-8)
Conformational energies of n-butane, n-pentane, and n-hexane have been
calculated at the CCSD(T) level and at or near the basis set limit.
Post-CCSD(T) contribution were considered and found to be unimportant. The data
thus obtained were used to assess the performance of a variety of density
functional methods. Double-hybrid functionals like B2GP-PLYP and B2K-PLYP,
especially with a small Grimme-type empirical dispersion correction, are
capable of rendering conformational energies of CCSD(T) quality. These were
then used as a `secondary standard' for a larger sample of alkanes, including
isopentane and the branched hexanes as well as key isomers of heptane and
octane. Popular DFT functionals like B3LYP, B3PW91, BLYP, PBE, and PBE0 tend to
overestimate conformer energies without dispersion correction, while the M06
family severely underestimates GG interaction energies. Grimme-type dispersion
corrections for these overcorrect and lead to qualitatively wrong conformer
orderings. All of these functionals also exhibit deficiencies in the conformer
geometries, particularly the backbone torsion angles. The PW6B95 and, to a
lesser extent, BMK functionals are relatively free of these deficiencies.
Performance of these methods is further investigated to derive conformer
ensemble corrections to the enthalpy function, , and the Gibbs
energy function, , of these alkanes. While
is only moderately sensitive to the level of theory, exhibits more pronounced sensitivity. Once again, double hybrids
acquit themselves very well.Comment: J. Phys. Chem. A, revised [Walter Thiel festschrift
Unraveling the performance of dispersion-corrected functionals for the accurate description of weakly bound natural polyphenols
Long-range non-covalent interactions play a key role in the chemistry of natural polyphenols. We have previously proposed a description of supramolecular polyphenol complexes by the B3P86 density functional coupled with some corrections for dispersion. We couple here the B3P86 functional with the D3 correction for dispersion, assessing systematically the accuracy of the new B3P86-D3 model using for that the well-known S66, HB23, NCCE31, and S12L datasets for non-covalent interactions. Furthermore, the association energies of these complexes were carefully compared to those obtained by other dispersion-corrected functionals, such as B(3)LYP-D3, BP86-D3 or B3P86-NL. Finally, this set of models were also applied to a database composed of seven non-covalent polyphenol complexes of the most interest.FDM acknowledges financial support from the Swedish Research Council (Grant No. 621-2014-4646) and SNIC (Swedish National Infrastructure for Computing) for providing computer resources. The work in Limoges (IB and PT) is supported by the âConseil RĂ©gional du Limousinâ. PT gratefully acknowledges the support by the Operational Program Research and Development Fund (project CZ.1.05/2.1.00/03.0058 of the Ministry of Education, Youth and Sports of the Czech Republic). IB gratefully acknowledges financial support from âAssociation Djerbienne en Franceâ
Modeling interstellar amorphous solid water grains by tight-binding based methods: comparison between GFN-XTB and CCSD(T) results for water clusters
One believed path to Interstellar Complexes Organic Molecules (iCOMs)
formation inside the Interstellar Medium (ISM) is through chemical
recombination at the surface of amorphous solid water (ASW) mantle covering the
silicate-based core of the interstellar grains. The study of these iCOMs
formation and their binding energy to the ASW, using computational chemistry,
depends strongly on the ASW models used, as different models may exhibit sites
with different adsorbing features. ASW extended models are rare in the
literature because large sizes require very large computational resources when
quantum mechanical methods based on DFT are used. To circumvent this problem,
we propose to use the newly developed GFN-xTB Semi-empirical Quantum Mechanical
(SQM) methods from the Grimme's group. These methods are, at least, two orders
of magnitude faster than conventional DFT, only require modest central memory,
and in this paper we aim to benchmark their accuracy against rigorous and
resource hungry quantum mechanical methods. We focused on 38 water structures
studied by MP2 and CCSD(T) approaches comparing energetic and structures with
three levels of GFN-xTB parametrization (GFN0, GFN1, GFN2) methods. The
extremely good results obtained at the very cheap GFN-xTB level for both water
cluster structures and energetic paved the way towards the modeling of very
large AWS models of astrochemical interest.Comment: 9 pages, 4 figures, Submitted to LNCS (Springer) ICCSA202
Elastic and vibrational properties of alpha and beta-PbO
The structure, electronic and dynamic properties of the two layered alpha
(litharge) and beta (massicot) phases of PbO have been studied by density
functional methods. The role of London dispersion interactions as leading
component of the total interaction energy between layers has been addressed by
using the Grimme's approach, in which new parameters for Pb and O atoms have
been developed. Both gradient corrected and hybrid functionals have been
adopted using Gaussian-type basis sets of polarized triple zeta quality for O
atoms and small core pseudo-potential for the Pb atoms. Basis set superposition
error (BSSE) has been accounted for by the Boys-Bernardi correction to compute
the interlayer separation. Cross check with calculations adopting plane waves
that are BSSE free have also been performed for both structures and vibrational
frequencies. With the new set of proposed Grimme's type parameters structures
and dynamical parameters for both PbO phases are in good agreement with
experimental data.Comment: 8 pages, 5 figure
Formation and destruction of polycyclic aromatic hydrocarbon clusters in the interstellar medium
The competition between the formation and destruction of coronene clusters
under interstellar conditions is investigated theoretically. The unimolecular
nucleation of neutral clusters is simulated with an atomic model combining an
explicit classical force field and a quantum tight-binding approach.
Evaporation rates are calculated in the framework of the phase space theory and
are inserted in an infrared emission model and compared with the growth rate
constants. It is found that, in interstellar conditions, most collisions lead
to cluster growth. The time evolution of small clusters (containing up to 312
carbon atoms) was specifically investigated under the physical conditions of
the northern photodissociation region of NGC 7023. These clusters are found to
be thermally photoevaporated much faster than they are reformed, thus providing
an interpretation for the lowest limit of the interstellar cluster size
distribution inferred from observations. The effects of ionizing the clusters
and density heterogeneities are also considered. Based on our results, the
possibility that PAH clusters could be formed in PDRs is critically discussed.Comment: 14 pages, 14 figures. Astronomy & Astrophysics, accepted for
publicatio
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