Breakdown of Valence Shell Electron Pair Repulsion Theory in an H-Bond-Stabilized Linear sp-Hybridized Sulfur

Exploring the unusual orbital hybridization types of atoms and their new connection modes contributes to the development of chemical bond theory and can inspire compounds with unique molecular configurations.Dicoordinated sulfur(S)atoms(or anions)with sp3 hybridization in a bent-bridging mode are commonly observed in many inorganic and organic compounds.However,sp-hybridized S species have,thus far,been extremely rare,and the linearly bridging mode has only been“forcibly”achieved with the aid of metal–S multiple bonds and/or significant steric hindrance from the surrounding organic ligands.

Tuning the Spatially Controlled Growth,Structural Self-Organizing and Cluster-Assembling of the Carbyne-Enriched Nano-Matrix during Ion-Assisted Pulse-Plasma Deposition

Carbyne-enriched nanomaterials are of current interest in nanotechnology-related applications.The properties of these nanomaterials greatly depend on their production process.In particular,structural self-organization and auto-synchronization of nanostructures are typical phenomena observed during the growth and heteroatom-doping of carbyne-enriched nanostructured metamaterials by the ion-assisted pulse-plasma deposition method.Accordingly,fine tuning of these processes may be seen as the key step to the predictive designing of carbyneenriched nano-matrices with improved properties.In particular,we propose an innovative concept,connected with application of the vibrational-acoustic effects and based on universal Cymatics mechanisms.These effects are used to induce vibration-assisted self-organized wave patterns together with the simultaneous manipulation of their properties through an electric field.Interaction between the inhomogeneous electric field distribution generated on the vibrating layer and the plasma ions serves as the additional energizing factor controlling the local pattern formation and self-organization of the nano-structures.

The preparation of whole sp-C composed alkyne rich carbon materials

For the high content of sp-hybridized carbon atoms,carbyne based materials can express superior conductivity and ultra-high theoretical capacity,which are key factors of high-performance anode.However,the poor stability of synthetic intermediates and unwanted side reactions lead to huge challenge to synthesis carbyne alternating carbon–carbon triple and single bonds.Here,we rationally designed a smart“Greedy Snake”strategy to synthesize the alkyne rich carbon materials named Si capped alkyne rich carbon(Si-Alkyne-C)which comprised of sp-hybridized carbon atoms.The as-prepared Si-Alkyne-C generated on the copper surface through a carbon–carbon coupling,in which Si can effectively protect the intermediates generated by the reaction.The C–Si bond can constantly generate copper-alkyne intermediates to couple with other terminal alkynes to continuously elongate like"Greedy Snake",forming a long alkyne chain structure.The as-prepared Si-Alkyne-C can be applied as anode electrodes,exhibited very high reversible capacity of up to 2776 mAh/g at a current density of 50 mA/g and an average capacity around 1202 mAh/g at a high current density of 5000 mA/g for 5000 cycles,which are the best results among the reported carbon materials and better than many other anode materials.These results not only provide a facile strategy to prepare carbyne based materials,but also open a broad avenue for the preparation of high-capacity anode materials.