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Dimethanospiro octaplane

C(C)4 have been found... 35 Two years later, Rasmussen and Radom30 designed the first stable ptC surrounded only by carbons, [ptC(C)4], the dimethanospiro[2,2]octaplane (Figure 3).30 Wang and Schleyer found a set of boron spiroalkanes with a ptC(C)4 through substitution of carbon by boron atoms.36,37 In 2003, a novel family of molecules based on a C( moiety was proposed by us, which constituted the simplest and smaller set of molecules containing a ptC(C)4, and more importantly, the first and, at that time, the only one stabilized purely by electronic factors.38... [Pg.253]

Fig. 1.6 Dimethanospiro[2.2] octaplane, 4. This is the calculated structure at the MP/6-31G(d) level... Fig. 1.6 Dimethanospiro[2.2] octaplane, 4. This is the calculated structure at the MP/6-31G(d) level...
This study of dimethanospiro[2.2]octaplane must leave tittle doubt that its central carbon is either perfectly planar, or that the barrier to planarization is very small, in which latter case the relative-minimum species probably has a nearly-planar central carbon (one longs for the day when computer power will permit a CCSD(T) [37,38] optimization/frequency calculation with a 6-31G(d) or bigger basis on a molecule like this). Radom and Rasmussen followed this discovery of the very promising... [Pg.6]

Fig. 1.7 Molecules 5 and 6 are closely related to dimethanospiro[2.2]octaplane but perhaps easier to synthesize 5 resembles closely the well-known pagodane, 7... Fig. 1.7 Molecules 5 and 6 are closely related to dimethanospiro[2.2]octaplane but perhaps easier to synthesize 5 resembles closely the well-known pagodane, 7...
Fig. 1.10 The cyclopropylidene and the allene from opening of the spiropentane moiety ofdime-thanospiro[2.2]octaplane. These are molecular mechanics structures. The cyclopropylidene structure shown here actually has the carbons of the three-membered ring and the two carbons of the double bond in the same positions as the corresponding carbons of the spiropentane moiety of dimethanospiro[2.2]octaplane, and so its function here is only heuristic (cf. Fig. 1.9)... Fig. 1.10 The cyclopropylidene and the allene from opening of the spiropentane moiety ofdime-thanospiro[2.2]octaplane. These are molecular mechanics structures. The cyclopropylidene structure shown here actually has the carbons of the three-membered ring and the two carbons of the double bond in the same positions as the corresponding carbons of the spiropentane moiety of dimethanospiro[2.2]octaplane, and so its function here is only heuristic (cf. Fig. 1.9)...
A series of computer experiments by Radom and Rasmussen iderrtified prorrrising candidates for perfectly-planar-carbon molectrles, the most prorrrising of which were dimethanospiro[2.2]octaplane arrd dimethanospiro[2.2]binorraplane. Becanse of their size, complexity, and the strain inctrrred by planar carborr, these compotrrtds represent formidable synthetic challenges nevertheless, it is conceivable that they could yield to a thorough retrosynthetic analysis followed by skillful implementation of one of the thus-revealed putative routes. [Pg.10]


See other pages where Dimethanospiro octaplane is mentioned: [Pg.254]    [Pg.3]    [Pg.3]    [Pg.4]    [Pg.5]    [Pg.6]    [Pg.7]    [Pg.8]    [Pg.9]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.5 , Pg.6 , Pg.7 , Pg.8 , Pg.9 ]




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Octaplane

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