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Tetrahedrane

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Tetrahedrane
Ball and stick model of tetrahedrane
Names
Preferred IUPAC name
Tricyclo[1.1.0.02,4]butane
Identifiers
3D model (JSmol)
2035811
ChEBI
ChemSpider
  • InChI=1S/C4H4/c1-2-3(1)4(1)2/h1-4H checkY
    Key: FJGIHZCEZAZPSP-UHFFFAOYSA-N checkY
  • C12C3C1C23
Properties
C4H4
Molar mass 52.076 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Tetrahedrane is a hypothetical platonic hydrocarbon with chemical formula C4H4 and a tetrahedral structure. The molecule would be subject to considerable angle strain and has not been synthesized as of 2023. However, a number of derivatives have been prepared. In a more general sense, the term tetrahedranes is used to describe a class of molecules and ions with related structure, e.g. white phosphorus.

Organic tetrahedranes

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In 1978, Günther Maier prepared tetra-tert-butyl-tetrahedrane.[1] The bulky tert-butyl (t-Bu) substituents envelop the tetrahedrane core. Maier suggested that bonds in the core are prevented from breaking because this would force the substituents closer together (corset effect) resulting in Van der Waals strain. Tetrahedrane is one of the possible platonic hydrocarbons and has the IUPAC name tricyclo[1.1.0.02,4]butane.

Unsubstituted tetrahedrane (C4H4) remains elusive, although it is predicted to be kinetically stable. One strategy that has been explored (but thus far failed) is reaction of propene with atomic carbon.[2] Locking away a tetrahedrane molecule inside a fullerene has only been attempted in silico.[3] Due to its bond strain and stoichiometry, tetranitrotetrahedrane has potential as a high-performance energetic material (explosive).[4] Some properties have been calculated based on quantum chemical methods.[5]

Tetra-tert-butyltetrahedrane

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This compound was first synthesised starting from a cycloaddition of an alkyne with t-Bu substituted maleic anhydride,[6] followed by rearrangement with carbon dioxide expulsion to a cyclopentadienone and its bromination, followed by addition of the fourth t-Bu group. Photochemical cheletropic elimination of carbon monoxide of the cyclopentadienone gives the target. Heating tetra-tert-butyltetrahedrane gives tetra-tert-butylcyclobutadiene. Though the synthesis appears short and simple, by Maier's own account, it took several years of careful observation and optimization to develop the correct conditions for the challenging reactions to take place. For instance, the synthesis of tetrakis(t-butyl)cyclopentadienone from the tris(t-butyl)bromocyclopentadienone (itself synthesized with much difficulty) required over 50 attempts before working conditions could be found.[7] The synthesis was described as requiring "astonishing persistence and experimental skill" in one retrospective of the work.[8] In a classic reference work on stereochemistry, the authors remark that "the relatively straightforward scheme shown [...] conceals both the limited availability of the starting material and the enormous amount of work required in establishing the proper conditions for each step."[9]

Tetra-tert-butyl-tetrahedrane synthesis 1978

Eventually, a more scalable synthesis was conceived, in which the last step was the photolysis of a cyclopropenyl-substituted diazomethane, which affords the desired product through the intermediacy of tetrakis(tert-butyl)cyclobutadiene:[10][11] This approach took advantage of the observation that the tetrahedrane and the cyclobutadiene could be interconverted (uv irradiation in the forward direction, heat in the reverse direction).

Tetra-tert-butyl-tetrahedrane synthesis 1991


Tetrakis(trimethylsilyl)tetrahedrane

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Tetrakis(trimethylsilyl)tetrahedrane is relatively stable

Tetrakis(trimethylsilyl)tetrahedrane can be prepared by treatment of the cyclobutadiene precursor with tris(pentafluorophenyl)borane[12] and is far more stable than the tert-butyl analogue. The silicon–carbon bond is longer than a carbon–carbon bond, and therefore the corset effect is reduced.[13] Whereas the tert-butyl tetrahedrane melts at 135 °C concomitant with rearrangement to the cyclobutadiene, tetrakis(trimethylsilyl)tetrahedrane, which melts at 202 °C, is stable up to 300 °C, at which point it cracks to bis(trimethylsilyl)acetylene.

The tetrahedrane skeleton is made up of banana bonds, and hence the carbon atoms are high in s-orbital character. From NMR, sp-hybridization can be deduced, normally reserved for triple bonds. As a consequence the bond lengths are unusually short with 152 picometers.

Reaction with methyllithium with tetrakis(trimethylsilyl)tetrahedrane yields tetrahedranyllithium.[14] Coupling reactions with this lithium compound gives extended structures.[15][16][17]

A bis(tetrahedrane) has also been reported.[18] The connecting bond is even shorter with 143.6 pm. An ordinary carbon–carbon bond has a length of 154 pm.

Synthesis of tetrakis(trimethylsilyl)tetrahedrane and its dimer.

Tetrahedranes with non-carbon cores

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In tetrasilatetrahedrane features a core of four silicon atoms. The standard silicon–silicon bond is much longer (235 pm) and the cage is again enveloped by a total of 16 trimethylsilyl groups, which confer stability. The silatetrahedrane can be reduced with potassium graphite to the tetrasilatetrahedranide potassium derivative. In this compound one of the silicon atoms of the cage has lost a silyl substituent and carries a negative charge. The potassium cation can be sequestered by a crown ether, and in the resulting complex potassium and the silyl anion are separated by a distance of 885 pm. One of the Si−–Si bonds is now 272 pm and the tetravalent silicon atom of that bond has an inverted tetrahedral geometry. Furthermore, the four cage silicon atoms are equivalent on the NMR timescale due to migrations of the silyl substituents over the cage.[19]

Tetrasilatetrahedrane

The dimerization reaction observed for the carbon tetrahedrane compound is also attempted for a tetrasilatetrahedrane.[20] In this tetrahedrane the cage is protected by four so-called supersilyl groups in which a silicon atom has 3 tert-butyl substituents. The dimer does not materialize but a reaction with iodine in benzene followed by reaction with the tri-tert-butylsilaanion results in the formation of an eight-membered silicon cluster compound which can be described as a Si2 dumbbell (length 229 pm and with inversion of tetrahedral geometry) sandwiched between two almost-parallel Si3 rings.

Silicon cluster compound

In eight-membered clusters of in the same carbon group, tin Sn8R6 and germanium Ge8R6 the cluster atoms are located on the corners of a cube.

Inorganic and organometallic tetrahedranes

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Structure of [InC(tms)3]4, a tetrahedrane with an In4 core (dark gray = In, orange = Si).[21]
Metal clusters that have tetrahedral cores are often called tetrahedranes.

The tetrahedrane motif occurs broadly in chemistry. White phosphorus (P4) and yellow arsenic (As4) are examples. Several metal carbonyl clusters are referred to as tetrahedranes, e.g. tetrarhodium dodecacarbonyl.

Metallatetrahedranes with a single metal (or phosphorus atom) capping a cyclopropyl trianion also exist.[22]

See also

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References

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  1. ^ Maier, G.; Pfriem, S.; Schäfer, U.; Matusch, R. (1978). "Tetra-tert-butyltetrahedrane". Angew. Chem. Int. Ed. Engl. 17 (7): 520–521. doi:10.1002/anie.197805201.
  2. ^ Nemirowski, Adelina; Reisenauer, Hans Peter; Schreiner, Peter R. (2006). "Tetrahedrane—Dossier of an Unknown". Chem. Eur. J. 12 (28): 7411–7420. doi:10.1002/chem.200600451. PMID 16933255.
  3. ^ Ren, Xiao-Yuan; Jiang, Cai-Ying; Wang, Jiang; Liu, Zi-Yang (2008). "Endohedral complex of fullerene C60 with tetrahedrane, C4H4@C60". J. Mol. Graph. Model. 27 (4): 558–562. doi:10.1016/j.jmgm.2008.09.010. PMID 18993098.
  4. ^ Zhou, Ge; Zhang, Jing-Lai; Wong, Ning-Bew; Tian, Anmin (2004). "Computational studies on a kind of novel energetic materials tetrahedrane and nitro derivatives". Journal of Molecular Structure: Theochem. 668 (2–3): 189–195. doi:10.1016/j.theochem.2003.10.054.
  5. ^ Jarowski, Peter D.; Diederich, Francois; Houk, Kendall N. (2005). "Structures and Stabilities of Diacetylene-Expanded Polyhedranes by Quantum Mechanics and Molecular Mechanics". Journal of Organic Chemistry. 70 (5): 1671–1678. doi:10.1021/jo0479819. PMID 15730286.
  6. ^ Maier, Günther; Boßlet, Friedrich (1972). "tert-Butyl-substituierte cyclobutadiene und cyclopentadienone" [tert-Butyl-substituted cyclobutadienes and cyclopentadienones]. Tetrahedron Letters. 13 (11): 1025–1030. doi:10.1016/S0040-4039(01)84500-7.
  7. ^ Maier, Günther; Pfriem, Stephan; Schäfer, Ulrich; Malsch, Klaus-Dieter; Matusch, Rudolf (December 1981). "Kleine Ringe, 38: Tetra-tert-butyltetrahedran". Chemische Berichte (in German). 114 (12): 3965–3987. doi:10.1002/cber.19811141218.
  8. ^ Lewars, Errol. (2008). Modeling marvels : computational anticipation of novel molecules. [Dordrecht]: Springer. ISBN 978-1-4020-6973-4. OCLC 314371890.
  9. ^ Eliel, Ernest L. (Ernest Ludwig), 1921-2008. (1994). Stereochemistry of organic compounds. Wilen, Samuel H., Mander, Lewis N. New York: Wiley. ISBN 0-471-01670-5. OCLC 27642721.{{cite book}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  10. ^ Maier, Günther; Fleischer, Frank (1991-01-01). "Ein alternativer zugang zum tetra-tert-butyltetrahedran". Tetrahedron Letters (in German). 32 (1): 57–60. doi:10.1016/S0040-4039(00)71217-2. ISSN 0040-4039.
  11. ^ Rubin, M.; Rubina, M.; Gevorgyan, V. (2006). "Recent Advances in Cyclopropene Chemistry". Synthesis. 2006 (8): 1221–1245. doi:10.1055/s-2006-926404.
  12. ^ Nakamoto, M.; Inagaki, Y.; Ochiai, T.; Tanaka, M.; Sekiguchi, A. (2011). "Cyclobutadiene to tetrahedrane: Valence isomerization induced by one-electron oxidation". Heteroatom Chemistry. 22 (3–4): 412–416. doi:10.1002/hc.20699.
  13. ^ Maier, Günther; Neudert, Jörg; Wolf, Oliver; Pappusch, Dirk; Sekiguchi, Akira; Tanaka, Masanobu; Matsuo, Tsukasa (2002). "Tetrakis(trimethylsilyl)tetrahedrane". J. Am. Chem. Soc. 124 (46): 13819–13826. doi:10.1021/ja020863n. PMID 12431112.
  14. ^ Sekiguchi, Akira; Tanaka, Masanobu (2003). "Tetrahedranyllithium: Synthesis, Characterization, and Reactivity". J. Am. Chem. Soc. 125 (42): 12684–5. doi:10.1021/ja030476t. PMID 14558797.
  15. ^ Nakamoto, Masaaki; Inagaki, Yusuke; Nishina, Motoaki; Sekiguchi, Akira (2009). "Perfluoroaryltetrahedranes: Tetrahedranes with Extended σ−π Conjugation". J. Am. Chem. Soc. 131 (9): 3172–3. doi:10.1021/ja810055w. PMID 19226138.
  16. ^ Ochiai, Tatsumi; Nakamoto, Masaaki; Inagaki, Yusuke; Sekiguchi, Akira (2011). "Sulfur-Substituted Tetrahedranes". J. Am. Chem. Soc. 133 (30): 11504–7. doi:10.1021/ja205361a. PMID 21728313.
  17. ^ Kobayashi, Y.; Nakamoto, M.; Inagaki, Y.; Sekiguchi, A. (2013). "Cross-Coupling Reaction of a Highly Strained Molecule: Synthesis of σ–π Conjugated Tetrahedranes". Angew. Chem. Int. Ed. 52 (41): 10740–10744. doi:10.1002/anie.201304770. PMID 24038655. S2CID 30151404.
  18. ^ Tanaka, M.; Sekiguchi, A. (2005). "Hexakis(trimethylsilyl)tetrahedranyltetrahedrane". Angew. Chem. Int. Ed. 44 (36): 5821–5823. doi:10.1002/anie.200501605. PMID 16041816.
  19. ^ Ichinohe, Masaaki; Toyoshima, Masafumi; Kinjo, Rei; Sekiguchi, Akira (2003). "Tetrasilatetrahedranide: A Silicon Cage Anion". J. Am. Chem. Soc. 125 (44): 13328–13329. doi:10.1021/ja0305050. PMID 14583007.
  20. ^ Fischer, G.; Huch, V.; Mayer, P.; Vasisht, S. K.; Veith, M.; Wiberg, N. (2005). "Si8(SitBu3)6: A Hitherto Unknown Cluster Structure in Silicon Chemistry". Angewandte Chemie International Edition. 44 (48): 7884–7887. doi:10.1002/anie.200501289. PMID 16287188.
  21. ^ Uhl, Werner; Graupner, Rene; Layh, Marcus; Schütz, Uwe (1995). "In4{C(SiMe3)3}4 mit In4-tetraeder und In4Se4{C(SiMe3)3}4 mit In4Se4-heterocubanstruktur". Journal of Organometallic Chemistry. 493 (1–2): C1–C5. doi:10.1016/0022-328X(95)05399-A.
  22. ^
    • Organometallics 2019, 38, 21, 4054–4059.
    • Organometallics 1984, 3, 1574−1583.
    • Organometallics 1986, 5, 25−33.
    • J. Am. Chem. Soc. 1984, 106, 3356−3357.
    • J. Chem. Soc., Chem. Commun. 1984, 485−486.
    • Science Advances 25 Mar 2020: Vol. 6, no. 13, doi:10.1126/sciadv.aaz3168
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