MS36-P17 Further Structural Adventures with Bis-metallacarboranesGeorgina Rosair(Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, United Kingdom)Alan Welch(Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, United Kingdom)Anthony Chan(Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, United Kingdom)email: G.M.Rosair@hw.ac.ukMetallacarboranes display great variation in polyhedral size and shape. They incorporate metal atoms from across the Periodic Table 1 and find application in catalysis, medicine, metal-ion extraction and advanced materials.1
The parent 1,1′-bis(ortho-carborane) (below) has a scaffold which offers extensive potential for derivatisation. Single cage metalation of 1,1′-bis(ortho-carborane) has yielded metallacarborane-carborane species,2 with double cage metalation affording metallacarborane-metallacarborane compounds.2 However such metalation follows double deboronation (removal of one vertex from each cage) so the final products are necessarily homometalated. Very recently stepwise deboronation and metalation of 1,1′-bis(ortho-carborane) has enabled the synthesis and characterisation of the first examples of heterometalated metallacarborane-metallacarborane species (one example below). More variety and surprises are revealed in this structural adventure with metallacarboranes.3 References:
1. Grimes, R. N. (2016) Carboranes, 3rd ed.; Elsevier: Amsterdam, The Netherlands.
2. Thiripuranathar, G.; Man, W. Y.; Palmero, C.; Chan, A. P. Y.; Leube, B. T.; Ellis, D.; McKay, D.; Macgregor, S. A.; Jourdan, L.; Rosair, G. M.; Welch, A. J. (2015) Dalton Trans., 44, 5628-5637.;.Thiripuranathar, G.; Chan, A. P. Y.; Mandal, D.; Man, W. Y.; Argentari, M.; Rosair, G. M.; Welch, A. J. (2017) Dalton Trans., 46, 1811-1821.
3. Chan, A. P. Y.; Rosair, G. M.; Welch, A. J. (2018) Inorg. Chem., submitted.