Huber, G ; Mitzel, Norbert W.UniBi ; Schier, A ; Schmidbauer, H
The structural chemistry of a series of triaminosilanes XSi(NR2)(3) has been investigated in order to determine the ground-state configuration and conformation of these molecules. Theoretical studies and analogy with the isoelectronic XP(NR2)(3) (X = CH2, O, Se, NSiMe3 etc.) and P(NR2)(3) molecules suggest structures of C-s or C-3 symmetry, with small energy differences between them. The molecular structure of HSi(NMe2)(3) (1) has been determined by a single-crystal X-ray diffraction study at low temperature. Surprisingly, the molecules have a non-standard conformation with an irregular orientation of the three NMe2 groups. The hydride-, chloro-, methyl-, and vinyltris(morpholino)silanes XSi[N(CH2CH2)(2)O](3) (X = H, Cl, Me, Vi; 2-5) were prepared from the corresponding chlorosilanes and morpholine (2, 3) or lithium morpholide (4, 5). Their variable-temperature NMR spectra were studied and the molecular structures determined by single crystal X-ray diffraction. Compound 2 has a molecular geometry approaching mirror symmetry with one morpholino group significantly different from the other two. This structure resembles that of isoelectronic tris(amino)phosphines. Compounds 3-5 have structures with a propeller-like arrangement of the three morpholino rings approaching C-3 symmetry for this part of the molecules. The chore compound 3 shows the shortest Si-N bond lengths (average 1.690 Angstrom), followed by 2 (1.708 Angstrom), 5 (1.709 Angstrom) and 4 (1.712 Angstrom). The configuration of all nitrogen atoms is almost planar, with sums of the angles close to 360 degrees, and the morpholino rings adopt a chair conformation. According to the solution NMR spectra the ring inversion is slow at low temperature, but the rings rotate freely about the Si-N bonds on the NMR time scale. The molecular structures are discussed in terms of steric and electronic effects of the substituents. Other model compounds, including (Me2N)(3)SiC6H4-4-Br (6), MeSi[N(CH2CH2)(2)NMe](3) (7) and PhSi[N(CH2)(4)](3) (8), could not be crystallized, but were characterized by their analytical and spectroscopic data.
Huber G, Mitzel NW, Schier A, Schmidbauer H. The molecular structures of triaminosilanes. CHEMISCHE BERICHTE-RECUEIL. 1997;130(8):1159-1166.
Huber, G., Mitzel, N. W., Schier, A., & Schmidbauer, H. (1997). The molecular structures of triaminosilanes. CHEMISCHE BERICHTE-RECUEIL, 130(8), 1159-1166.
Huber, G., Mitzel, N. W., Schier, A., and Schmidbauer, H. (1997). The molecular structures of triaminosilanes. CHEMISCHE BERICHTE-RECUEIL 130, 1159-1166.
Huber, G., et al., 1997. The molecular structures of triaminosilanes. CHEMISCHE BERICHTE-RECUEIL, 130(8), p 1159-1166.
G. Huber, et al., “The molecular structures of triaminosilanes”, CHEMISCHE BERICHTE-RECUEIL, vol. 130, 1997, pp. 1159-1166.
Huber, G., Mitzel, N.W., Schier, A., Schmidbauer, H.: The molecular structures of triaminosilanes. CHEMISCHE BERICHTE-RECUEIL. 130, 1159-1166 (1997).
Huber, G, Mitzel, Norbert W., Schier, A, and Schmidbauer, H. “The molecular structures of triaminosilanes”. CHEMISCHE BERICHTE-RECUEIL 130.8 (1997): 1159-1166.
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