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Hydrocarbon analogues of boron clusters--planarity, aromaticity and antiaromaticity.

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TLDR
Experimental and theoretical evidence is reported that small boron clusters prefer planar structures and exhibit aromaticity and antiaromaticity according to the Hückel rules, akin to planar hydrocarbons.
Abstract
An interesting feature of elemental boron and boron compounds is the occurrence of highly symmetric icosahedral clusters. The rich chemistry of boron is also dominated by three-dimensional cage structures. Despite its proximity to carbon in the periodic table, elemental boron clusters have been scarcely studied experimentally and their structures and chemical bonding have not been fully elucidated. Here we report experimental and theoretical evidence that small boron clusters prefer planar structures and exhibit aromaticity and antiaromaticity according to the Huckel rules, akin to planar hydrocarbons. Aromatic boron clusters possess more circular shapes whereas antiaromatic boron clusters are elongated, analogous to structural distortions of antiaromatic hydrocarbons. The planar boron clusters are thus the only series of molecules other than the hydrocarbons to exhibit size-dependent aromatic and antiaromatic behaviour and represent a new dimension of boron chemistry. The stable aromatic boron clusters may exhibit similar chemistries to that of benzene, such as forming sandwich-type metal compounds.

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Experimental realization of two-dimensional boron sheets

TL;DR: Experimental work is presented showing that two-dimensional boron sheets can be grown epitaxially on a Ag(111) substrate and density functional theory simulations agree well with experiments, and indicate that both sheets are planar without obvious vertical undulations.
Journal ArticleDOI

Developing paradigms of chemical bonding: adaptive natural density partitioning.

TL;DR: A method of description of the chemical bonding combining the compactness and intuitive simplicity of Lewis theory with the flexibility and generality of canonical molecular orbital theory is presented, which is called adaptive natural density partitioning.
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Observation of an all-boron fullerene.

TL;DR: The observation of an all-boron fullerene-like cage cluster at B40(-) with an extremely low electron-binding energy is reported, by photoelectron spectroscopy, and theoretical calculations show that this arises from a cage structure with a large energy gap, but that a quasi-planar isomer of B40 (-) with two adjacent hexagonal holes is slightly more stable than the fullerenes structure.
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Graphene-analogous low-dimensional materials

TL;DR: In this paper, the authors summarize the recent progress on graphene-analogous low-dimensional materials (2D nanosheets and 1D nanoribbons) from both experimental and computational side, and emphasis is placed on structure, properties, preparation, and potential applications of graphene analogous materials as well as the comparison with graphene.
References
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Journal ArticleDOI

Accurate and simple analytic representation of the electron-gas correlation energy

TL;DR: A simple analytic representation of the correlation energy for a uniform electron gas, as a function of density parameter and relative spin polarization \ensuremath{\zeta}, which confirms the practical accuracy of the VWN and PZ representations and eliminates some minor problems.
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Advanced Inorganic Chemistry

TL;DR: Cotton and Wilkinson's Advanced Inorganic Chemistry (AIC) as discussed by the authors is one of the most widely used inorganic chemistry books and has been used for more than a quarter century.
Journal ArticleDOI

Au20: A Tetrahedral Cluster

TL;DR: Using relativistic density functional calculations, it is found that Au20 possesses a tetrahedral structure, which is a fragment of the face-centered cubic lattice of bulk gold with a small structural relaxation, which suggests that the Au20 cluster should be highly stable and chemically inert.
Journal ArticleDOI

On the calculation of multiplet energies by the hartree-fock-slater method

TL;DR: In this article, a consistent application of the p1/3 approximation of the Hartree-Fock-Slater method requires the use of one specific procedure, the sum method, for the calculation of the energy of singlet excited states of closed shell molecules.
Journal ArticleDOI

Implementation of time-dependent density functional response equations

TL;DR: The implementation of the relevant equations in the Amsterdam Density Functional program is described and certain aspects of the implementation which are necessary for an efficient evaluation of the desired properties, enabling the treatment of large molecules are focused on.
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