Neutral counting assigns five electrons to cyclopentadienyl ligand and two to CO. Thus each fragment has valence electrons and contributes three skeletal electrons; each fragment has sixteen and contributes four:For A the six-pair four-vertex count is the nido count derived from a five-vertex trigonal bipyramid. Removing an axial vertex leaves a tetrahedron: the three equatorial vertices plus the remaining axial vertex. For B the corresponding arachno fragment is obtained by removing both axial vertices from that same parent, leaving a three-metal triangle. Small clusters require specifying the parent and removed vertices; mechanically calling every nido fragment a square pyramid is wrong.
The Fe tetramer is indeed known to have a tetrahedral core, with four face-capping CO groups. The carbon atoms of those carbonyls and the iron atoms form interpenetrating tetrahedra, giving a cubane-like Fe–C connectivity. Bridging rather than terminal CO changes the distribution of local donation, not the total electron count above.[ref]
Structural Characterization of the Cyclopentadienyliron Carbonyl Tetramer, Fe4(eta5-C5H5)4(CO)4. A Cubane-Type Structure Containing a Completely Bonding Tetrametal Cluster Unit by Melvin A. Neuman and others. 1972, pp.3383–3388, tetrahedral iron core and face-capping carbonyls
For a neutral borane with one terminal B–H bond assigned to each vertex, the skeletal electron number is ; an overall charge adds electrons. Suitable twelve-electron correspondences areFor C, four BH contributions plus four additional hydrogens give electrons. For D, three BH contributions plus five additional hydrogens and the negative charge give . They map to the tetrahedral and triangular low-vertex skeletons respectively. The neutral formal alternative for D is , also with twelve skeletal electrons.
The electron counting correspondence alone must not be read as evidence that the neutral boranes are isolable stable bulk materials. Low-vertex hydrogen-rich boranes can be transient; the triangular octahydrotriborate anion is the established practical three-boron example, whereas neutral is a formal analogy rather than an equally established preparative product. The requested skeletal correspondence should be distinguished from a claim about comparable stability or isolation conditions.[ref]
Reactions of the octahydrotriborate(1-) anion, B3H8-, with some complexes of cobalt(I), cobalt(II), rhodium(I), and iridium(I), and the characterization of the borallyl complex IrIII(eta3-B3H7)(CO)H(PPh3)2 by Norman N. Greenwood and others. 1980, pp.196–200, reactions of the preparatively accessible octahydrotriborate anion
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