Please find below few refs, in the topic of your question. Most probably there has an answer:
1. Inorganic Chemistry, 53, 2014, 9284-9295; Synthesis, structure, and catalytic applications for ortho - And meta -carboranyl based NBN pincer-Pd complexes; Tsang, M., Viñas, C., Teixidor, F., Planas, J., Conde, N., Sanmartin, R., Herrero, M., Domínguez, E., Lledos, A., Vidossich, P., Choquesillo-Lazarte, D.
2. Chemistry - A European Journal, 20, 2014, 3120-3127, Structural and photophysical study on heterobimetallic complexes with d8-d10 interactions supported by carborane ligands: Theoretical analysis of the emissive behaviour, Crespo, O., Gimeno, M., Laguna, A., Lehtonen, O., Ospino, I., Pyykkö, P., Villacampa, M.
3. Journal of the American Chemical Society, 135, 2013, 12192-12195
Palladium-catalyzed selective fluorination of o-carboranes (Article)
Qiu, Z., Quan, Y., Xie, Z.
4. Accounts of Chemical Research, 44, 2011, 299-309, Transition metal-carboryne complexes: Synthesis, bonding, and reactivity, Qiu, Z., Ren, S., Xie, Z.
5. Journal of the American Chemical Society, 132, 2010, 16085-16093
Palladium/nickel-cocatalyzed cycloaddition of 1,3-dehydro-o-carborane with alkynes. Facile synthesis of C,B-substituted carboranes, Qiu, Z., Xie, Z.
Thanks for your reply. I am new to this chemistry. I am using the following protocol from literature. Let me explain my doubt again.
I am analyzing my synthesized carborane derivatives with a Pd-Stain which is having PdCl2, water and Conc. HCl. I usually spot my compound on TLC glass plate and I run it in suitable solvent. Later, I am immersing the TLC in Pd-stain and drying rapidly in hot air. I can able to see some dark spots in TLC.
So, please explain me what actually happening between my carborane derivative and Pd-stain here?
Only thing I know that some reduction reaction is happening here. But, I do not know the relevant particulars about it. Please explain me.