Carbon nanotubes (CNTs) have generated a tremendous amount of research interest because of their unique structural, electronic, magnetic, and mechanical properties. [1] Among the various synthetic methods employed for their preparation, chemical vapor deposition (CVD) has emerged to be most effective, and efforts are increasing in applying this technique to pre-growth device fabrication by utilizing (in particular lithographically) [2] patterned catalyst arrays and in situ tube assembly. [2,3] Crucial in this endeavor is the sitespecific batch production of ordered carbon with control of stoichiometry and ultimately morphology. One possible approach to achieving this would be the efficient thermal conversion of a defined, soluble, molecular organometallic precursor composed of both the carbon source and the metal catalyst, placed locospecifically by wetting and drying. Such a strategy would combine the advantages of the floating organometallic catalyst (for example, ferrocene, [Fe(CO) 5 ], etc.) CVD methodology [1d, 4] with a solid-state conversion of carbon precursors. Reports of the latter reveal some serious shortcomings with respect to yield and/or degree of graphitization, extremity of conditions, need for specialized equipment, the requirement of co-reagents, and simplicity of starting materials. [1d, 5] We have described the solid-state thermolysis of a [Co 2 (CO) 6 ]-complexed tetrabenzodehydro [20]annulene and some of its substructures to form ordered carbon material, but this method shared some of these drawbacks, in as much as the highest yields were only about 60 %. The desired product consisted of an (at best) approximately equal mixture of multiwalled tubes (MWNTs)