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== Structure and Bonding ==
== Structure and Bonding ==
The parent iminoborane, HB=NH, is produced by the photolysis of H<sub>3</sub>BNH<sub>3</sub>.<ref>{{Cite journal|last1=Lory|first1=Earl R.|last2=Porter|first2=Richard F.|date=1973-03-01|title=Infrared studies of matrix isolated species in the hydrogen-boron-nitrogen system|journal=Journal of the American Chemical Society|volume=95|issue=6|pages=1766–1770|doi=10.1021/ja00787a012|issn=0002-7863}}</ref><ref>{{Cite journal|last1=Paetzold|first1=Peter|last2=Richter|first2=Anette|last3=Thijssen|first3=Theo|last4=Würtenberg|first4=Stefan|date=1979-12-01|title=Bildung, Struktur und Reaktivität von (Pentafluorphenyl)bor-tert-butylimid und seinem Cyclodimeren|journal=Chemische Berichte|language=en|volume=112|issue=12|pages=3811–3827|doi=10.1002/cber.19791121207|issn=1099-0682}}</ref><ref>{{Cite journal|last1=Paetzold|first1=Peter|last2=von Plotho|first2=Christoph|date=1982-08-01|title=Über weitere monomere Borimide und ihre Reaktionen|journal=Chemische Berichte|language=en|volume=115|issue=8|pages=2819–2825|doi=10.1002/cber.19821150813|issn=1099-0682}}</ref> Bonding in iminoboranes can be described by two [[Resonance (chemistry)|resonance structures]]:<ref>{{Cite journal|last1=Mó|first1=Otilia|last2=Yáñez|first2=Manuel|last3=Pendás|first3=Angel Martín|last4=Bene|first4=Janet E. Del|last5=Alkorta|first5=Ibon|last6=Elguero|first6=José|date=2007-07-23|title=Unusual substituent effects on the bonding of iminoboranes|url=http://xlink.rsc.org/?DOI=B702480K|journal=Phys. Chem. Chem. Phys.|language=en|volume=9|issue=30|pages=3970–3977|doi=10.1039/b702480k|pmid=17646885|bibcode=2007PCCP....9.3970M|issn=1463-9084|hdl=10261/72489}}</ref>
The parent iminoborane, HB=NH, is produced by the photolysis of H<sub>3</sub>BNH<sub>3</sub>.<ref>{{Cite journal|last1=Lory|first1=Earl R.|last2=Porter|first2=Richard F.|date=1973-03-01|title=Infrared studies of matrix isolated species in the hydrogen-boron-nitrogen system|journal=Journal of the American Chemical Society|volume=95|issue=6|pages=1766–1770|doi=10.1021/ja00787a012|issn=0002-7863}}</ref><ref>{{Cite journal|last1=Paetzold|first1=Peter|last2=Richter|first2=Anette|last3=Thijssen|first3=Theo|last4=Würtenberg|first4=Stefan|date=1979-12-01|title=Bildung, Struktur und Reaktivität von (Pentafluorphenyl)bor-tert-butylimid und seinem Cyclodimeren|journal=Chemische Berichte|language=en|volume=112|issue=12|pages=3811–3827|doi=10.1002/cber.19791121207|issn=1099-0682}}</ref><ref>{{Cite journal|last1=Paetzold|first1=Peter|last2=von Plotho|first2=Christoph|date=1982-08-01|title=Über weitere monomere Borimide und ihre Reaktionen|journal=Chemische Berichte|language=en|volume=115|issue=8|pages=2819–2825|doi=10.1002/cber.19821150813|issn=1099-0682}}</ref> Bonding in iminoboranes can be described by two [[Resonance (chemistry)|resonance structures]]:<ref>{{Cite journal|last1=Mó|first1=Otilia|last2=Yáñez|first2=Manuel|last3=Pendás|first3=Angel Martín|last4=Bene|first4=Janet E. Del|last5=Alkorta|first5=Ibon|last6=Elguero|first6=José|date=2007-07-23|title=Unusual substituent effects on the bonding of iminoboranes|url=http://xlink.rsc.org/?DOI=B702480K|journal=Phys. Chem. Chem. Phys.|language=en|volume=9|issue=30|pages=3970–3977|doi=10.1039/b702480k|pmid=17646885|bibcode=2007PCCP....9.3970M|issn=1463-9084|hdl=10261/72489}}</ref>
:HB<sup>-</sup><big>≡</big>N<sup>+</sup>H <big>↔</big> HB=NH
:HB<sup>-</sup><big><big><big>≡</big></big></big>N<sup>+</sup>H <big><big>↔</big></big> HB=NH


The stability is dramatically affected by bulkyy substituents such that one stable iminoborane is (tert-Bu)B=N(tert-Bu).<ref name=PPaetz>{{Cite journal|doi=10.1002/cber.19841170324|title=Darstellung, Reaktionen und Struktur vontert-Butyl(tert-butylimino)boran|year=1984|last1=Paetzold|first1=Peter|last2=Plotho|first2=Christoph Von|last3=Schmid|first3=Günter|last4=Boese|first4=Roland|last5=Schrader|first5=Bernhard|last6=Bougeard|first6=Daniel|last7=Pfeiffer|first7=Uwe|last8=Gleiter|first8=Rolf|last9=Schüfer|first9=Wolfgang|journal=Chemische Berichte|volume=117|pages=1089–1102}}</ref>
The stability is dramatically affected by bulkyy substituents such that one stable iminoborane is (tert-Bu)B=N(tert-Bu).<ref name=PPaetz>{{Cite journal|doi=10.1002/cber.19841170324|title=Darstellung, Reaktionen und Struktur vontert-Butyl(tert-butylimino)boran|year=1984|last1=Paetzold|first1=Peter|last2=Plotho|first2=Christoph Von|last3=Schmid|first3=Günter|last4=Boese|first4=Roland|last5=Schrader|first5=Bernhard|last6=Bougeard|first6=Daniel|last7=Pfeiffer|first7=Uwe|last8=Gleiter|first8=Rolf|last9=Schüfer|first9=Wolfgang|journal=Chemische Berichte|volume=117|pages=1089–1102}}</ref>

Revision as of 00:41, 12 November 2020

Structure of tBuN=B-tBu (tBu = tert-butyl). The B-N bond distance is 126 pm.[1]

Iminoboranes comprise a group of inorganic compounds with the generic formula containing triple bonds XB≡NY, where X, Y can be H, F, RO, R2N, R3C, etc, among which the simplest form is HB≡NH. They are electronically related to acetylenes but are usually more reactive due to the polarity.[2][3][4]

Structure and Bonding

The parent iminoborane, HB=NH, is produced by the photolysis of H3BNH3.[5][6][7] Bonding in iminoboranes can be described by two resonance structures:[8]

HB-≡N+H ↔ HB=NH

The stability is dramatically affected by bulkyy substituents such that one stable iminoborane is (tert-Bu)B=N(tert-Bu).[1]

Synthesis

Thermal decomposition of azidoboranes induces migration of R from boron to the nascent nitrene gives iminoboranes:[9]

R2B-N3 → RB=NR + N2

Elimination of fluorosilanes provides another route. Bulky substituents such as (Me3Si)3Si stabilize the iminoborane with respect to oligomerization:[10]

(Me3Si)3SiB(F)-N(SiMe3)2 → (Me3Si)3Si-B=N-SiMe3 + F-SiMe3

Reactivity

Oligomerization

Iminoboranes tend to oligomerize, often forming cyclic derivatives. Five types of oligomerization product are produced: cyclodimers (1,3,2,4-diazadiboretidines,[1] Di[11]), cyclotrimers (borazines, Tr), bicyclotrimers (Dewar borazines, Tr’[12]), cyclotetramers (octahydro-1,3,5,7-tetraza-2,4,6,8-tetraborocines, Te[13]), and polymers (polyiminoboranes, Po); which are shown below.[14] Which product is dominant depends on the structures of reactants and the reaction conditions. Some of the products can be interconverted.[15]

Addition reactions

Some electron-rich iminoboranes form adducts with Lewis acids.[16]

The addition of protic agents is a fast quantitive reaction.[17]

Boration reaction of iminoboranes is the addition of B-X single bond to B≡N, where -X can be -Cl (chloro-boration), -N3 (azido-boration), -SR (thio-boration), -NR2 (amino-boration) and R (alkyl-boration). One of these reactions are illustrated here.

Cycloaddition

The typical [2+3]-cycloaddition is the addition of B≡N and RN3 to give a BN4 ring.[1] One of the widely investigated [2+2]-cycloadditions is the reaction of aldehydes and ketones.<ref>von Kutepow, Nikolaus (1972-04-01). "Chemistry of acetylenes. Von H. G. Viehe. Marcel Dekker Inc., New York 1969. 1. Aufl., XV, 1298 S., zahlr. Tab. u. Formeln, geb. $ 59.50". Angewandte Chemie. 84 (8): 367. doi:10.1002/ange.19720840843. ISSN 1521-3757.</ref

Coordination to transition metals

Like acetylenes, iminoboranes can also coordinate with transition metals.

References

  1. ^ a b c d Paetzold, Peter; Plotho, Christoph Von; Schmid, Günter; Boese, Roland; Schrader, Bernhard; Bougeard, Daniel; Pfeiffer, Uwe; Gleiter, Rolf; Schüfer, Wolfgang (1984). "Darstellung, Reaktionen und Struktur vontert-Butyl(tert-butylimino)boran". Chemische Berichte. 117: 1089–1102. doi:10.1002/cber.19841170324.
  2. ^ Inorganic ring systems : 7th International symposium : Papers. Chivers, Tristram. Gordon and Breach Science Publishers. 1994. ISBN 978-2-88449-168-6. OCLC 81135356.{{cite book}}: CS1 maint: others (link)
  3. ^ Advances in inorganic chemistry. Volume 31. Emeléus, H. J. (Harry Julius), Sharpe, A. G. New York: Academic Press. 1987. ISBN 978-0-12-023631-2. OCLC 277086713.{{cite book}}: CS1 maint: others (link)
  4. ^ Paetzold, Peter (1987). Iminoboranes. Advances in Inorganic Chemistry. Vol. 31. pp. 123–170. doi:10.1016/s0898-8838(08)60223-8. ISBN 978-0-12-023631-2.
  5. ^ Lory, Earl R.; Porter, Richard F. (1973-03-01). "Infrared studies of matrix isolated species in the hydrogen-boron-nitrogen system". Journal of the American Chemical Society. 95 (6): 1766–1770. doi:10.1021/ja00787a012. ISSN 0002-7863.
  6. ^ Paetzold, Peter; Richter, Anette; Thijssen, Theo; Würtenberg, Stefan (1979-12-01). "Bildung, Struktur und Reaktivität von (Pentafluorphenyl)bor-tert-butylimid und seinem Cyclodimeren". Chemische Berichte. 112 (12): 3811–3827. doi:10.1002/cber.19791121207. ISSN 1099-0682.
  7. ^ Paetzold, Peter; von Plotho, Christoph (1982-08-01). "Über weitere monomere Borimide und ihre Reaktionen". Chemische Berichte. 115 (8): 2819–2825. doi:10.1002/cber.19821150813. ISSN 1099-0682.
  8. ^ Mó, Otilia; Yáñez, Manuel; Pendás, Angel Martín; Bene, Janet E. Del; Alkorta, Ibon; Elguero, José (2007-07-23). "Unusual substituent effects on the bonding of iminoboranes". Phys. Chem. Chem. Phys. 9 (30): 3970–3977. Bibcode:2007PCCP....9.3970M. doi:10.1039/b702480k. hdl:10261/72489. ISSN 1463-9084. PMID 17646885.
  9. ^ Paetzold, Peter; Eleftheriadis, Eleftherios; Minkwitz, Rolf; Wölfel, Volker; Gleiter, Rolf; Bischof, Peter; Friedrich, Gert (1988-01-01). "Bildung, Struktur und Reaktionen von Methyl(methylimino)boran". Chemische Berichte. 121 (1): 61–66. doi:10.1002/cber.19881210110. ISSN 1099-0682.
  10. ^ Haase, Martin; Klingebiel, Uwe (1985-04-01). "Simple Synthesis of Stable Iminoboranes". Angewandte Chemie International Edition in English. 24 (4): 324. doi:10.1002/anie.198503241. ISSN 1521-3773.
  11. ^ Hess, H. (1969-11-15). "Strukturbestimmungen an Bor–Stickstoff-Verbindungen. IV. Die Kristall- und Molekularstruktur von Hexakis(trimethylsilyl)-2,4-diamino-1,3,2,4-diazadiboretidin" (PDF). Acta Crystallographica Section B (in German). 25 (11): 2342–2349. doi:10.1107/s056774086900567x. ISSN 0567-7408.
  12. ^ Steuer, Holger-A.; Meller, Anton; Elter, Gernot (1985). "B-t-butyl-borazine und -diazadiboretidine". Journal of Organometallic Chemistry. 295 (1): 1–6. doi:10.1016/0022-328x(85)88065-7.
  13. ^ Turner H. S. and Warne R. J. 1962 Proc. Chem. Soc. 69.
  14. ^ Advances in inorganic chemistry. Volume 31. Emeléus, H. J. (Harry Julius), Sharpe, A. G. New York: Academic Press. 1987. ISBN 978-0-12-023631-2. OCLC 277086713.{{cite book}}: CS1 maint: others (link)
  15. ^ Maier.G. (1978). "Tetra-tert-butyltetrahedrane". Angew. Chem. Int. Ed. Engl. 17: 520. doi:10.1002/anie.197805201.
  16. ^ Nöth, Heinrich; Weber, Siegfried (1985-06-01). "Beiträge zur Chemie des Bors, 158. Addukte von Aluminium- und Galliumhalogeniden an ein Aminoiminoboran". Chemische Berichte. 118 (6): 2554–2556. doi:10.1002/cber.19851180631. ISSN 1099-0682.
  17. ^ Nöth, Heinrich; Weber, Siegfried (1985-05-01). "Beiträge zur Chemie des Bors, 154. Addition von Trimethylsily-Verbindungen und von anderen Elektrophilen an (tert-Butylimino) (tetramethylpiperidino)boran". Chemische Berichte. 118 (5): 2144–2146. doi:10.1002/cber.19851180536. ISSN 1099-0682.
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