Oxoborane (RBO) Complexation and Concomitant Electrophilic Bond Activation Processes.

Donor-acceptor complexes of the oxoboranes ClB=O and HOB=O were synthesized and each feature short multiply bonded B=O linkages. The retention of high Lewis acidic character within these encapsulated monomeric oxoboranes was manifested by their ability to support C-F and Si-O bond activation/functionalization. The reported ClB=O complexes can be regarded as synthetic surrogates of the [BO] cation, an inorganic analogue of CO.

Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N)].

A donor-acceptor complex of HBNH was prepared thermolysis of a carbene-stabilized azidoborane. The reactivity of the fundamentally important HBNH unit (inorganic alkyne analogue) was explored in detail, including attempts to convert this species and related hydrido(azido)borane cations into molecular complexes of BN. This work provides added impetus for the development of molecular precursors that can release bulk boron nitride (a desirable insulator and thermal conductor) under mild conditions, and from solution.

Azido- and amido-substituted gallium hydrides supported by N-heterocyclic carbenes.

Despite recent advances in main group N-heterocyclic carbene (NHC) coordination chemistry, gallium hydrides remain, in large part, an unexplored area of research. In this paper we outline efficient routes to azide- and amido-functionalized gallium hydrides such as NHC·GaHN and NHC·GaHN(SiMe) and explore these species as potential precursors to HGaNH complexes and bulk gallium nitride (GaN).

Transition metal-mediated donor-acceptor coordination of low-oxidation state Group 14 element halides.

The reactivity of tungsten carbonyl adducts of Group 14 element (Ge, Sn and Pb) dihalides towards the metal-based donors (η(5)-C5H5)Rh(PMe2Ph)2 and Pt(PCy3)2 was examined. When (η(5)-C5H5)Rh(PMe2Ph)2 was treated with the Lewis acid supported Ge(ii) complex, THF·GeCl2·W(CO)5, cyclopentadienyl ring activation occurred, whereas the analogous Lewis acidic units SnCl2·W(CO)5 and PbCl2 form direct adducts with the Rh complex to yield Rh-Sn and Rh-Pb dative bonds. Attempts to prepare metal coordinated element(ii) hydrides by adding hydride sources to the above mentioned rhodium-E(ii) halide complexes were unsuccessful; in each case insoluble products were formed along with regeneration of free (η(5)-C5H5)Rh(PMe2Ph)2.

Direct Evaluation of the Quantum Confinement Effect in Single Isolated Ge Nanocrystals.

To address the yet open question regarding the nature of quantum confinement in Ge nanocrystals (Ge NCs) we employed scanning tunneling spectroscopy to monitor the electronic structure of individual isolated Ge NCs as a function of their size. The (single-particle) band gaps extracted from the tunneling spectra increase monotonically with decreasing nanocrystal size, irrespective of the capping ligands, manifesting the effect of quantum confinement. Band-gap widening of ∼1 eV with respect to the bulk value was observed for Ge-NCs 3 nm in diameter.

Encapsulating Inorganic Acetylene, HBNH, Using Flanking Coordinative Interactions.

A stable donor-acceptor coordination complex of the elusive parent inorganic iminoborane HBNH (a structural analogue of acetylene) is reported. This species was generated via thermally induced N2 elimination/1,2-H migration from a hydrido(azido)borane adduct NHC⋅BH2N3 (NHC=N-heterocyclic carbene) in the presence of a fluorinated triarylborane. The mechanism of this process was also investigated by computational and isotopic labeling studies.

One-pot synthesis of functionalized germanium nanocrystals from a single source precursor.

One-pot syntheses of surface functionalized germanium nanocrystals (GeNCs) based upon traditional hot injection and microwave-assisted heating of a Ge(II) dihydride single source precursor have been developed. The reported procedures offer in situ hydrogermylation-based covalent attachment of alkene/alkyne derived surface moieties that give access to hydrophobic or hydrophilic GeNCs.

Application of the donor-acceptor concept to intercept low oxidation state group 14 element hydrides using a Wittig reagent as a Lewis base.

This article outlines our attempts to stabilize the Group 14 element dihydrides, GeH2 and SnH2, using commonly employed phosphine and pyridine donors; in each case, elemental Ge and Sn extrusion was noted. However, when these phosphorus and nitrogen donors were replaced with the ylidic Wittig ligand Ph3P═CMe2, stable inorganic methylene complexes (EH2) were obtained, demonstrating the utility of this under-explored ligand class in advancing main group element coordination chemistry.