|This article relies largely or entirely upon a single source. (December 2013)|
|Jmol-3D images||Image 1|
|Molar mass||260.37 g mol−1|
|Dipole moment||0 D|
|Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)|
Pagodane is an organic compound with formula C
20 whose carbon skeleton was said to resemble a pagoda, hence the name. It is a polycyclic hydrocarbon whose molecule has the D2h point symmetry group. The compound is a highly crystalline solid that melts at 243 °C, is barely soluble in most organic solvents and moderately soluble in benzene and chloroform. It sublimes at low pressure.
The name pagodane is used more generally for any member of a family of compounds whose molecular skeletons have the same 16-carbon central cage as the basic compound. Each member can be seen as the result of connecting eight atoms of this cage in pairs by four alkane chains. The general member is denoted [m.n.p.q]pagodane where m, n, p and q are the number of carbons of those four chains. The general formula is then C
12+2s where s= m+n+p+q. In particular, the basic compound C
20 has those carbons connected by four methylene bridges (m=n=p=q=1), and its name within that family is therefore [18.104.22.168]pagodane.
Synthesis and structure
The compound was first synthesized by H. Prinzbach et al. in 1987, by a 14-step sequence starting from isodrin. In the process they also synthesized [22.214.171.124]pagodane C
24 and several derivatives.
Prinzbach and co-workers remarked that "the obvious need for [the short name 'pagodane'] can be readily understood in view of the von Baeyer/IUPAC and Chemical Abstracts nomenclature", undecacyclo[9.9.0.01,5.02,12.02,18.03,7.06,10.08,12.011,15.013,17.316,20]icosane.
Eight of pagodane's 20 carbon atoms (numbered 3,5,8,10,13,15,18, and 20) have an inverted tetrahedral geometry as in some propellanes – specifically, [2.2.1]propellane, whose carbon skeleton is a part of pagodane's.
Both [126.96.36.199]pagodane and [188.8.131.52]pagodane form divalent cations in SbF
2ClF. In these cations the electron deficiency is spread over the central cyclobutane ring. These dications were the first examples to show the phenomenon of σ-bishomoaromaticity which was subsequently studied by the Prizbach group to great length.
- Wolf-Dieter Fessner, Gottfried Sedelmeier, Paul R. Spurr, Grety Rihs, H. Prinzbach (1987), "Pagodane": the efficient synthesis of a novel, versatile molecular framework. J. Am. Chem. Soc., volume 109 issue 15, pp. 4626–42 doi:10.1021/ja00249a029
- G. K. Surya Prakash (1998), Investigations on intriguing long lived carbodications. Pure & Appl. Chem., volume 70 issue 10, pp. 2001–06. Online version at iupac.org accessed on 2010-01-14. doi:10.1351/pac199870102001
- G.K.S. Prakash, V.V. Krishnamurthy, R. Herges, R. Bau, H. Yuan, G.A Olah, W.-D. Fessner, H. Prinzbach: [184.108.40.206]- and [220.127.116.11]Pagodane Dications: Frozen Two-Electron Woodward-Hoffmann Transition State Models. J. Am. Chem. Soc. 1988, 110, 7764-7772
- Wolf-Dieter Fessner, Bulusu A. R. C. Murty, Horst Prinzbach (1987), The Pagodane Route to Dodecahedranes – Thermal, Reductive, and Oxidative Transformations of Pagodanes Angewandte Chemie International Edition in English Volume 26, Issue 5, pp. 451–52 doi:10.1002/anie.198704511
- Wolf-Dieter Fessner, Bulusu A. R. C. Murty, Jürgen Wörth, Dieter Hunkler, Hans Fritz, Horst Prinzbach, Wolfgang D. Roth, Paul von Ragué Schleyer, Alan B. McEwen, Wilhelm F. Maier (1987), Dodecahedranes from [18.104.22.168]Pagodanes. Angewandte Chemie International Edition in English, Volume 26, Issue 5, pp. 452–54 doi:10.1002/anie.198704521