@article {161, title = {Carborane-thiol protected copper nanoclusters: Stimuli-responsive materials with tunable phosphorescence}, journal = {Chemical Science}, volume = {14}, year = {2023}, month = {12/2023}, pages = {1613-1626}, type = {Article}, chapter = {1613}, abstract = {

Atomically precise nanomaterials with tunable solid-state luminescence attract global interest. In this work, we present a new class of thermally stable isostructural tetranuclear copper nanoclusters (NCs), shortly Cu4@oCBT, Cu4@mCBT and Cu4@ICBT, protected by nearly isomeric carborane thiols: ortho-carborane-9-thiol, meta-carborane-9-thiol and ortho-carborane 12-iodo 9-thiol, respectively. They have a square planar Cu4 core and a butterfly-shaped Cu4S4 staple, which is appended with four respective carboranes. For Cu4@ICBT, strain generated by the bulky iodine substituents on the carboranes makes the Cu4S4 staple flatter in comparison to other clusters. High-resolution electrospray ionization mass spectrometry (HR ESI-MS) and collision energy-dependent fragmentation, along with other spectroscopic and microscopic studies confirm their molecular structure. Although none of these clusters show any visible luminescence in solution, bright μs-long phosphorescence is observed in their crystalline forms. The Cu4@oCBT and Cu4@mCBT NCs are green emitting with quantum yields (Ф) of 81 and 59 \%, respectively, whereas Cu4@ICBT is orange emitting with a Φ of 18 \%. Density functional theory (DFT) calculations reveal the nature of their respective electronic transitions. The green luminescence of Cu4@oCBT and Cu4@mCBT clusters get shifted to yellow after mechanical grinding, but it is regenerated after exposure to solvent vapour, whereas the orange emission of Cu4@ICBT is not affected by mechanical grinding. Structurally flatten Cu4@ICBT didn{\textquoteright}t show mechonoresponsive luminescence in contrast to other clusters, having bent Cu4S4 structures. Cu4@oCBT and Cu4@mCBT are thermally stable up to 400 {\textdegree}C. The Cu4@oCBT retained green emission even upon heating to 200 {\textdegree}C under ambient conditions, while Cu4@mCBT changed from green to yellow in the same window. This is the first report on structurally flexible carborane thiol appended Cu4 NCs having stimuli-responsive tunable solid-state phosphorescence.

}, keywords = {boron, Cluster, Copper, Cu4L4, Phosphorescence, Responsive}, doi = {https://doi.org/10.1039/D2SC06578A}, url = {https://pubs.rsc.org/en/content/articlelanding/2023/sc/d2sc06578a}, author = {Arijit Jana and Madhuri Jash and Wakeel Ahmed Dar and Jayoti Roy and Papri Chakraborty and Paramasivam Ganesan and Sergei Lebedkin and Kaplan Kirakci and Sujan Manna and P. K. Sudhadevi Antharjanam and Jan Machacek and Monika Kucerakova and Sundargopal Ghosh and Kamil Lang and Manfred Kappes and Tomas Base and T. Pradeep} } @article {123, title = {Reversible Capture of Small Molecules On Bimetallaborane Clusters: Synthesis, Structural Characterization, and Photophysical Aspects}, journal = {Inorganic Chemistry}, volume = {50}, year = {2011}, chapter = {7511}, doi = {10.1021/ic200374k}, url = {http://pubs.acs.org/doi/abs/10.1021\%2Fic200374k}, author = {Jonathan Bould and Tomas Base and Michael G S Londesborough and Luis A Oro and Ramon Macias and John D Kennedy and Pavel Kubat and Marcel Fuciman and Tomas Polivka and Kamil Lang} } @article {117, title = {Carborane-thiol-silver interactions. A comparative study of the molecular protection of silver surfaces}, journal = {Surface and Coatings Technology}, volume = {204}, year = {2010}, chapter = {2639}, abstract = {

The interaction between flat silver surfaces and carboranethiol derivatives, and its relevance regarding the molecular protection of silver against corrosion by hydrogen sulphide, are reported here. A comparison of the protective qualities of four carboranethiols (1-HS-1,2-C2B10H11, 1,2-(HS)2-1,2-C2B10H10, 9,12-(HS)2-1,2-C2B10H10, and 1,12-(HS)2-1,2-C2B10H10) with several organic thiols (1-butanethiol, 1-octanethiol, 1-dodecanethiol, benzene-1,2-dithiol, benzenethiol, and sodium 2-mercaptoethanesulphonate) is provided. All these derivatives are categorized according to their capacity to inhibit the interaction of silver with H2S in the presence of water molecules in the gas phase. We found that significantly better molecular protection for silver surfaces is afforded by the carboranethiol derivatives, and, of these, 9,12-(HS)2-1,2-C2B10H10 proved to be particularly effective. The corrosion of silver by H2S is accompanied by well-defined colour changes from lustrous silver, through yellow, violet, blue, and finally to grey. This sequence has not been reported before and it is used in this study as a qualitative indicator of the extent of silver corrosion. Our results are supported by reflectance UV

}, doi = {10.1016/j.surfcoat.2010.02.019}, url = {http://www.sciencedirect.com/science/article/pii/S0257897210001106}, author = {Tomas Base and Zdenek Bastl and Vladimir Havranek and Kamil Lang and Jonathan Bould and Michael G S Londesborough and Jan Machacek and Jaromir Plesek} } @article {160, title = {Carborane-thiol protected copper nanoclusters: Stimuli-responsive materials with tunable phosphorescence }, journal = {Chemical Science}, abstract = {

Atomically precise nanomaterials with tunable solid-state luminescence attract global interest. In this work, we present a new class of thermally stable isostructural tetranuclear copper nanoclusters (NCs), shortly Cu4@oCBT, Cu4@mCBT and Cu4@ICBT, protected by nearly isomeric carborane thiols: ortho-carborane-9-thiol, meta-carborane-9-thiol and ortho-carborane 12-iodo 9-thiol, respectively. They have a square planar Cu4 core and a butterfly-shaped Cu4S4 staple, which is appended with four respective carboranes. For Cu4@ICBT, strain generated by the bulky iodine substituents on the carboranes makes the Cu4S4 staple flatter in comparison to other clusters. High-resolution electrospray ionization mass spectrometry (HR ESI-MS) and collision energy-dependent fragmentation, along with other spectroscopic and microscopic studies confirm their molecular structure. Although none of these clusters show any visible luminescence in solution, bright μs-long phosphorescence is observed in their crystalline forms. The Cu4@oCBT and Cu4@mCBT NCs are green emitting with quantum yields (Ф) of 81 and 59 \%, respectively, whereas Cu4@ICBT is orange emitting with a Φ of 18 \%. Density functional theory (DFT) calculations reveal the nature of their respective electronic transitions. The green luminescence of Cu4@oCBT and Cu4@mCBT clusters get shifted to yellow after mechanical grinding, but it is regenerated after exposure to solvent vapour, whereas the orange emission of Cu4@ICBT is not affected by mechanical grinding. Structurally flatten Cu4@ICBT didn{\textquoteright}t show mechonoresponsive luminescence in contrast to other clusters, having bent Cu4S4 structures. Cu4@oCBT and Cu4@mCBT are thermally stable up to 400 {\textdegree}C. The Cu4@oCBT retained green emission even upon heating to 200 {\textdegree}C under ambient conditions, while Cu4@mCBT changed from green to yellow in the same window. This is the first report on structurally flexible carborane thiol appended Cu4 NCs having stimuli-responsive tunable solid-state phosphorescence.

}, keywords = {boron, carborane, Cluster, Copper, Phosphorescence, Responsive, thiol}, doi = {https://doi.org/10.1039/D2SC06578A}, url = {https://pubs.rsc.org/en/content/articlelanding/2023/sc/d2sc06578a}, author = {Arijit Jana and Madhuri Jash and Wakeel A Dar and Jayoti Roy and Papri Chakraborty and Paramasivam Ganesan and Sergei Lebedkin and Kaplan Kirakci and Sujan Manna and P. K. Sudhadevi Antharjanam and Jan Machacek and Monika Kucerakova and Sundargopal Ghosh and Kamil Lang and Manfred Kappes and Tomas Base and T. Pradeep} }