Stannylene Synthesis

Stannylenes (R₂Sn:) are a class of organotin(II) compounds that are analogues of carbene. Unlike carbene, which usually has a triplet ground state, stannylenes have a singlet ground state since valence orbitals of tin (Sn) have less tendency to form hybrid orbitals and thus the electrons in 5s orbital are still paired up. Free stannylenes are stabilized by steric protection. Adducts with Lewis bases are also known.

History

The first persistent stannylene, Me₃Si)₂CHsub>2Sn, was reported by Michael F. Lappert in 1973. Lappert used the same synthetic approach to synthesize the first diamidostannylene Me₃Si)₂Nsub>2Sn in 1974.

The short-lived, transient stannylene Me₂Sn has been generated by thermolysis of ''cyclo''-(Me₂Sn)₆.

Synthesis and characterization

Persistent stannylene

Most alkyl stannylenes have been synthesized by alkylation of tin(II) dihalides with organolithium reagents. For example, the first stannylene, Me₃Si)₂CHsub>2Sn, was synthesized using (Me₃Si)₂CHLi and SnCl₂.

In some cases, stannylenes have been prepared by reduction of a tin(IV) compound by KC₈

Amidostannylene can also be synthesized by using a tin(II) dihalide and the lithium amide.

Short-lived stannylene

The isolation of a transient alkyl stannylene is more difficult. The first isolation of dimethylstannylene was believed to be done by thermolysing cyclostannane (Me₂Sn)₆, which was the product of the condensation of Me₂Sn(NEt₂)₂ and Me₂SnH₂. The evidence came from the vibrational frequencies of dimethylstannylene identified by infrared spectroscopy, which is consistent with the calculated value. The existence of this elusive SnMe₂ was further confirmed by the discovery of visible light absorption matching the calculated electronic transition of SnMe₂ in gas phase.

Another method to prepare short-lived stannylene is laser flash photolysis using tetraalkyltin(IV) compound (e.g. SnMe₄) as a precursor. The generation of stannylene can be monitored by transient UV-VIS spectroscopy.

Structure and bonding

Stannylenes can be viewed as sp²-hybridized with vacant 5p orbital and a lone pair. This gives rise to their red color from n to p transition.

With specific type of ligands, the electron deficiency of monomeric stannylene is reduced by the agostic interaction from B-H bond. This concept was proved by Mark Kenyon and coworkers in 2006 when they synthesized the cyclic dialkylstannylene Me₃Si)CCH₂sub>2Sn. The crystal structure of the synthesized compound showed the arrangement of one B-H bond toward the Sn atom with the B—H--Sn bond distance of 2.03 Å. The mitigation of Sn electron deficiency was proved by the spectroscopic data, especially the ¹¹⁹Sn NMR spectra which showed the drastically low chemical shift (587 and 787 ppm comparing to 2323 ppm in analogous dialkylstannylene) indicating more electron density around Sn in this case.

Reactivity

Oligomerization

Small, unstable stannylenes (e.g. dimethylstannylene) undergo self-oligomerization yielding cyclic oligostannanes, which can be used as stannylene sources.

More bulky stannylenes (e.g. Lappert's stannylene), on the other hand, tend to form a dimer. The nature of the Sn-Sn bond in stannylene dimer is rather different from C-C bond in carbene dimer (i.e. alkene). As alkene develops a typical double bond character and the molecule has a planar geometry, stannylene dimer has a trans-bent geometry. The double bond in stannylene dimer can be considered as two donor-acceptor interactions. The electron localization function (ELF) analysis of stannylene dimer shows a disynaptic basin (electrons in bonding orbitals) on both Sn atom, indicating that the interaction between two Sn atom is two unusual bent dative bonds. Apart from that, the stability of stannylene dimer is also affected by the steric repulsion and dispersion attraction between bulky substituents.

Insertion reaction

Alkylstannylenes can react with various reagents (e.g. alkyl halides, enones, dienes) in an oxidative addition (or insertion) fashion. The reaction between stannylene and 9,10-phenanthrolinedione produces an EPR signal that was identified to be 9,10-phenanthrenedione radical anion, indicating that this reaction proceeds ''via'' radical mechanism.

Cycloaddition

Although stannylenes are more stable than its lighter carbene analogs, they readily undergo +4cycloaddition reaction with Z-alkenes. The addition of (CH(SiMe₃)₂)₂Sn, to 2,7-diphenylocta-2,3,5,6-tetraene proceeds in a cheletropic fashion, as allowed by Woodward-Hoffmann rules.

Metal center for oxidative addition and reductive elimination

In terms of the Sn^II/Sn^IV couple, certain stannylenes resemble transition metals. The singlet-triplet energy separation is considered to have a strong effect on oxidative addition reactivity, by utilizing a very strong σ-donor boryl (-BX₂) ligand. The results demonstrated that not only molecular hydrogen but also E-H bond (E = B, Si, O, N) can be oxidative added on Sn. In ammonia and water cases, the oxidative added product could also undergo reductive elimination, yielding O- or N-B bond formation.

See also

*Carbene analogs
*Silylene

References

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Organotin compounds
Tin(II) compounds
Substances discovered in the 1970s
Octet-deficient functional groups