I think it's ruthenium(IV) oxide with a substituted propylenediamine ligand chelated to it. (this is a polydentate ligand, coordinating with its 4 nitrogens)
I wonder what that 2 part is about, it seems to indicate two perchlorate groups, but I have no idea how that would fit in.. perhaps its a bridging ligand (but how would the charge balance?)
I'm just guessing here, but I think one would have to prepare this compound--not purchase it. Unless you've got access to Sigma/Fischer/Aldrich, and a fair amount of money to spend on ruthenium salts (they're not terribly expensive--but not terribly cheap either)... don't even bother thinking twice about this reagent... and if you did have such access, you'd just buy a drum or twelve of GBL anyhow.
RuO2(ClO4)2 with the substituted diamine coordinated to it makes sense if the ruthenium is 6+... Rhodium is absolutely right. Sorry about my dyslexia. :)
Full text to the above-mentioned article:Synthesis, Electrochemistry, and Reactivities of trans-[Ru(L)O2]2+ (L = N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)propylenediamineChi-Ming Che, Wai-Tong Tang, and Chi-Keung LiJ. Chem. Soc. Dalton Trans 3735-3739 (1990) (https://www.thevespiary.org/rhodium/Rhodium/pdf/thf2gbl.ruo2l2.pdf)
(https://www.thevespiary.org/rhodium/Rhodium/pdf/thf2gbl.ruo2l2.pdf)
AbstractThe synthesis and characterization of the ligand N,N'-dimethyl-N,N'-
bis(2-pyridylmethyl)propylenediamine (L) and the complex
trans-[Ru(L)O
2]
2+ are described. The complex has been characterized by uv-visible [d
xy ? d
?* (d
?* = d
xz,d
yz) at 380-420 nm] and IR [V
asym(RuO
2) at 860 cm
-1] spectroscopy. At pH 1.0 it exhibits three reversible couples Ru
VI-Ru
IV Ru
IV-Ru
III, and Ru
III-Ru
II at potentials of 0.89, 0.60, and 0.28 V respectively vs. saturated calomel electrode. The Ru
VI-Ru
IV couple splits into two reversible one-electron couples Ru
VI-Ru
V and Ru
V-Ru
IV in alkaline solutions (pH > 9). The complex is a powerful oxidant, capable of oxidizing toluene to benzaldehyde, alcohols to aldehydes/ketones, tetrahydrofuran to ?-butyrolactone, and norbornene to exo-2,3-epoxy-norbornane in high yields at room temperature. Oxidation of cis- and trans-stilbenes gave benzaldehyde and trans-stilbene oxides.