Skip to main content
NCBI home page
ACS AuthorChoice logoLink to ACS AuthorChoice
. 2011 Jul 11;30(15):3930–3938. doi: 10.1021/om1011159

Conformational Control of Polysilanes: Use of CH2 Spacers in the Silicon Backbone

Andreas Wallner 1, Johann Hlina 1, Harald Wagner 1, Judith Baumgartner 1,*, Christoph Marschner 1,*
PMCID: PMC3148124  PMID: 21818170

Abstract

graphic file with name om-2010-011159_0003.jpg

By the reaction of a number of oligosilyl potassium compounds with (trimethylsilyl)chloromethane, derivatives containing the (trimethylsilyl)methyl substituent were prepared. Using X-ray single-crystal structure analysis and UV spectroscopy the conformational properties of some of the compounds were studied. It was found that the (trimethylsilyl)methylated examples exhibit UV absorption properties which correspond to lower energy transitions in comparison to those of analogous trimethylsilylated molecules. The influence of this effect decreases, however, with increasing chain lengths.

Introduction

In recent years small alkylated polysilanes(1) have been used to investigate the conformational dependency of the σ-bond electron delocalization of these compounds.2−8 Some reports have dealt with branched derivatives of this substance class, which were either dendrimers9−14 or linear silanes with branched end groups.15−17 Comparing oligosilanes containing either tris(trimethylsilyl)silyl or bis(trimethylsilyl)methylsilyl groups as terminating units, Krempner and Köckerling found that less branched silanes exhibited bathochromically shifted low-energy absorptions.(18) Our own studies, on the other hand, showed that the steric bulk of end groups is of importance for an all-transoid alignment of the main chain of polysilanes.16,19,20

With these two facts in mind, we decided to utilize the (trimethylsilyl)methyl group(21) in order to have the electronic properties of a methyl group which nevertheless is bulky enough to exercise sufficient steric influence onto the attached oligosilane unit. While these were the initial considerations for the synthesis of oligosilanes containing the (trimethylsilyl)methyl group, it later turned out that these materials were the most interesting starting materials for an AlCl3-catalyzed rearrangement desilylative cyclization process, which leads to methylene containing cyclo- and bicyclosilanes.(22)

Results and Discussion

Synthesis

Reaction of [tris(trimethylsilyl)silyl]potassium(23) (1) with (trimethylsilyl)chloromethane gave tris(trimethylsilyl)[(trimethylsilyl)methyl]silane (2) in almost quantitative yield (Scheme 1). In a similar way 2 could also be converted easily to the corresponding trisilanylpotassium compound 3 by reaction with potassium tert-butoxide. Introduction of another (trimethylsilyl)methyl group was achieved again with (trimethylsilyl)chloromethane, yielding 2,2-bis[(trimethylsilyl)methyl]hexamethyltrisilane (4), which can be considered as a larger version of octamethyltrisilane. The additional steric bulk of 4 allowed us to obtain the disilanylpotassium compound 5 by removal of another trimethylsilyl group. Previous attempts to achieve the same transformation starting from octamethyltrisilane failed, likely because of the higher kinetic reactivity of (pentamethyldisilanyl)potassium.(23) The reaction of 5 with (trimethylsilyl)chloromethane leading to 1,1,1-tris[(trimethylsilyl)methyl]trimethyldisilane (6) (Scheme 1) concluded the series of incremental introductions of the (trimethylsilyl)methyl group.

Scheme 1. Successive Replacement of Trimethylsilyl by (Trimethylsilyl)methyl Groups.

Scheme 1

Open in a new tab

[Bis(trimethylsilyl)((trimethylsilyl)methyl)silyl]potassium (3) was then used to obtain further derivatives containing the bis(trimethylsilyl)[(trimethylsilyl)methyl]silyl group (Scheme 2). Oxidative coupling with 1,2-dibromoethane gave 1,2-bis[(trimethylsilyl)methyl]tetrakis(trimethylsilyl)disilane (7). Reaction with either pentamethylchlorodisilane or tris(trimethylsilyl)chlorosilane provided the expected compounds 13 and 14 as the products of salt elimination. When 3 was reacted with α,ω-dichloromethyloligosilanes, two bis(trimethylsilyl)[(trimethylsilyl)methyl]silyl groups were connected with methylated silanylene spacers of different lengths (8–10) (Scheme 2).

Scheme 2.

Scheme 2

Open in a new tab

Further treatment of 14 with potassium tert-butoxide led to selective removal of a trimethylsilyl group from the more highly silylated silicon atom. The silylpotassium compound that formed was treated with either dimethyl sulfate or pentamethylchlorodisilane to give the respectively substituted derivatives 15 and 16 (Scheme 3).

Scheme 3.

Scheme 3

Open in a new tab

In order to extend the series of permethyloligosilanylene-bridged compounds 8–10, 1,6-bis[tris(trimethylsilyl)silyl]dodecamethylhexasilane16,19 was converted into the 1,8-dianionic derivative, which upon treatment with (trimethylsilyl)chloromethane gave 11 (Scheme 4). In a similar way 1,2-bis[tris(trimethylsilyl)silyl]tetramethyldisilane24,25 was converted into the monopotassium species, which was then converted to a derivative with one (trimethylsilyl)methyl group (17) (Scheme 4).

Scheme 4.

Scheme 4

Open in a new tab

Crystal Structure Analyses

Single-crystal structure analyses could be obtained for 7–10 and 12. Compound 7 (Figure 1) crystallizes in the triclinic space group P1̅ with an inversion center between the central Si–Si bond, in contrast to the case for hexakis(trimethylsilyl)disilane, which crystallizes in the trigonal space group R3̅c.26−29 The replacement of a trimethylsilyl group with a (trimethylsilyl)methyl group diminishes steric strain, as indicated by the shortening of the central Si–Si bond from 2.40 Å to 2.39 Å. This also affects the dihedral angle Me3Si–Si–Si–SiMe3, which would be 60° in a perfectly staggered conformation; the angles deviate to 43.3 and 76.6° in hexakis(trimethylsilyl)disilane,26−29 whereas the values for 7 are 51.5 and 65.0°.

Figure 1.

Figure 1

Open in a new tab

Molecular structure and numbering of 7 with 30% probability thermal ellipsoids. Hydrogen atoms are omitted for clarity. Selected bond lengths (Å) and bond angles (deg) with esd's: Si(1)–C(1) = 1.908(3), Si(1)–Si(2) = 2.3683(12), Si(1)–Si(3) = 2.3764(12), Si(1)–Si(1A) = 2.3864(19), Si(2)–C(2) = 1.872(3); C(1)–Si(1)–Si(2) = 117.34(9), C(1)–Si(1)–Si(3) = 107.86(9), Si(2)–Si(1)–Si(3) = 105.38(4), C(1)–Si(1)–Si(1A) = 107.10(9), Si(2)–Si(1)–Si(1A) = 109.99(5), Si(3)–Si(1)–Si(1A) = 108.93(5), Si(4)–C(1)–Si(1) = 126.46(14).

Compound 8 (Figure 2) and 1,1,1,4,4,4-hexakis(trimethylsilyl)tetramethyltetrasilane(30) both crystallize in the triclinic space group P1̅. However, while in the latter the inversion center resides at the middle of the central Si–Si bond, there is no symmetry in the asymmetric unit of 8. As a consequence of this, 1,1,1,4,4,4-hexakis(trimethylsilyl)tetramethyltetrasilane displays an all-transoid aligned conformation, whereas in 8 the torsion angle along the central Si–Si bond (Si(2)–Si(3)–Si(4)–Si(5)) is the rather unusual 129°. This can be seen from a Newman projection of 8 along the Si–Si skeleton, which shows an eclipsed conformation of the trimethylsilyl groups of the two branched shells for 8, whereas 1,1,1,4,4,4-hexakis(trimethylsilyl)tetramethyltetrasilane(30) has a staggered conformation.

Figure 2.

Figure 2

Open in a new tab

Molecular structure and numbering of 8 with 30% probability thermal ellipsoids. Hydrogen atoms are omitted for clarity. Selected bond lengths (Å)] and bond angles (deg) with esd’s: Si(1)–C(1) = 1.874(6), Si(1)–Si(2) = 2.358(2), Si(2)–C(4) = 1.911(6), Si(2)–Si(7) = 2.365(2), Si(2)–Si(3) = 2.367(2), Si(5)–C(9) = 1.894(6), Si(8)–C(4) = 1.860(6), Si(10)–C(9) = 1.861(7); C(4)–Si(2)–Si(1) = 120.36(19), Si(1)–Si(2)–Si(7) = 106.77(8), Si(1)–Si(2)–Si(3) = 108.84(9), Si(7)–Si(2)–Si(3) = 106.62(9), Si(2)–Si(3)–Si(4) = 114.51(9), Si(5)–Si(4)–Si(3) = 115.07(9), Si(6)–Si(5)–Si(4) = 110.08(9), C(9)–Si(5)–Si(9) = 102.1(2), Si(6)–Si(5)–Si(9) = 107.27(9), Si(4)–Si(5)–Si(9) = 107.56(9), Si(8)–C(4)–Si(2) = 125.4(3), Si(10)–C(9)–Si(5) = 124.1(3).

Compound 9 (Figure 3), with three dimethylsilylene units as a spacer, crystallizes in the monoclinic space group P21/c with two molecules in the asymmetric unit. One of the two molecules exhibited a disorder in one of the bis(trimethylsilyl)[(trimethylsilyl)methyl]silyl parts which required a number of restraints to resolve. Compound 10 (Figure 4), with four dimethylsilylene units as a spacer, crystallizes in the monoclinic space group P21/n. No unusually elongated Si–Si bonds were found. For the parent compound 1,1,1,6,6,6-hexakis(trimethylsilyl)octamethylhexasilane crystallization in the triclinic space group P1̅ and a staggered conformation with respect to the tris(trimethylsilyl)silyl groups were found.(15)

Figure 3.

Figure 3

Open in a new tab

Molecular structure and numbering of 9 with 30% probability thermal ellipsoids. Hydrogen atoms are omitted for clarity. Selected bond lengths (Å) and bond angles (deg) with esd’s: Si(1)–Si(2) = 2.368(2), Si(2)–C(16) = 1.879(6), Si(1)–C(3) = 1.873(6), Si(2)–Si(3) = 2.358(2), Si(6)–C(20) = 1.919(6), Si(6)–Si(11) = 2.379(2); C(16)–Si(2)–Si(3) = 117.1(2), C(16)–Si(2)–Si(1) = 109.6(2), Si(3)–Si(2)–Si(1) = 109.49(9), C(16)–Si(2)–Si(8) = 103.5(2), Si(3)–Si(2)–Si(8) = 111.77(9), Si(1)–Si(2)–Si(8) = 104.60(9), C(20)–Si(6)–Si(5) = 113.39(19), C(20)–Si(6)–Si(7) = 117.16(19), Si(5)–Si(6)–Si(7) = 107.77(9), C(20)–Si(6)–Si(11) = 103.59(19), Si(5)–Si(6)–Si(11) = 109.24(8), Si(7)–Si(6)–Si(11) = 105.09(8).

Figure 4.

Figure 4

Open in a new tab

Molecular structure and numbering of 10 with 30% probability thermal ellipsoids. Hydrogen atoms are omitted for clarity. Selected bond lengths (Å)] and bond angles (deg) with esd’s: Si(1)–Si(2) = 2.3629(12), Si(2)–C(11) = 1.907(3), Si(2)–Si(3) = 2.3708(12), Si(2)–Si(5) = 2.3736(14), Si(3)–Si(4) = 2.3696(12), Si(4)–Si(4A) = 2.3562(15), Si(6)–C(11) = 1.875(3); C(11)–Si(2)–Si(1) = 114.71(10), C(11)–Si(2)–Si(3) = 113.13(10), Si(1)–Si(2)–Si(3) = 110.39(4), C(11)–Si(2)–Si(5) = 103.06(10), Si(1)–Si(2)–Si(5) = 105.20(4), Si(3)–Si(2)–Si(5) = 109.70(5), Si(4)–Si(3)–Si(2) = 114.77(4), Si(4A)–Si(4)–Si(3) = 110.01(5), Si(6)–C(11)–Si(2) = 124.74(16).

In contrast to what was found for 8, compounds 9 (the two crystallographically independent molecules show similar conformational properties) and 10 (which has an inversion center at the central Si–Si bond and hence a central torsion angle of 180°) feature all-transoid conformations with torsion angles close to 160°, which shows that with a growing number of dimethylsilylene spacers along the silicon skeleton the effect of the (trimethylsilyl)methyl group is diminishing.

Compound 12 (Figure 5), with a 1,4-butanylene group as a spacer, crystallizes in the monoclinic space group C2/c. The structures of bis[tris(trimethylsilyl)silyl]methane,(31) bis[tris(trimethylsilyl)silyl]ethane,(32) and bis[tris(trimethylsilyl)silyl]propane(32) were determined before. The Si(1)–C(1) bond length in 12 (1.92 Å) is comparable to that in the other three structures mentioned above. The Si(1)–C(1)–C(2) bond angle of 117.8° is reduced compared to 136.2° in bis[tris(trimethylsilyl)silyl]methane, 119.9° in bis[tris(trimethylsilyl)silyl]ethane, and 118.1° in bis[tris(trimethylsilyl)silyl]propane. As in 10, a staggered conformation with respect to the tris(trimethylsilyl)silyl groups was found in 12.

Figure 5.

Figure 5

Open in a new tab

Molecular structure and numbering of 12 with 30% probability thermal ellipsoids. Hydrogen atoms are omitted for clarity. Selected bond lengths (Å) and bond angles (deg) with esd’s: Si(1)–C(1) = 1.920(5), Si(1)–Si(2) = 2.352(2), Si(1)–Si(4) = 2.357(2), Si(1)–Si(3) = 2.362(2), Si(2)–C(5) = 1.890(7), C(1)–C(2) = 1.533(8), C(2)–C(2A) = 1.532(11); C(1)–Si(1)–Si(2) = 106.45(18), C(1)–Si(1)–Si(4) = 109.57(18), Si(2)–Si(1)–Si(4) = 108.02(8), C(2)–C(1)–Si(1) = 117.7(4), C(2A)–C(2)–C(1) = 113.7(6).

Spectroscopy

1H, 13C, and 29Si NMR spectra of all new compounds were obtained and followed the expected trends for branched oligosilanes. Only the (trimethylsilyl)methyl group exhibited a very distinct spectroscopic pattern. For a 4-fold alkylated silicon atom a resonance close to 0 is expected in the 29Si spectrum. Typically the respective peak was found at around +1.6 ppm for neutral compounds. In the proton and carbon spectra the methylene unit exhibited typical signatures with 1H resonances ranging from −0.10 to +0.24 and 13C values clustered around −6.5 ppm. The only exception from the 13C trend can be found for compounds 4 and 6, where two and three (trimethylsilyl)methyl groups are on the same silicon atom, and compounds 7 and 14, both of which are sterically rather demanding branched compounds. The stronger steric strain present in these four compounds seems to be reflected in the observed downfield shifts.

As outlined in the Introduction, we were particularly interested in the UV absorption properties of the (trimethylsilyl)methylated oligosilanes compared to those of their trimethylsilylated parent compounds. The fact that silyl substituents cause an increase in the absorption energy can easily be recognized by a comparison of trisilanes. While tetrakis(trimethylsilyl)silane and tris(trimethylsilyl)methylsilane both have their lowest energy absorption maxima below 210 nm, the corresponding band for octamethyltrisilane can be found at 215 nm.(33) Similar to that, we found the absorption band of 2 at 211 nm, whereas the double-(trimethylsilyl)methylated 4 exhibits a bathochromically shifted band at 222 nm.

Rather spectacular changes can be observed when the absorption spectra of permethyloligosilanylene-bridged bis[tris(trimethylsilyl)silyl] compounds(19) are compared to the respective derivatives where two of the terminal trimethylsilyl groups are replaced by (trimethylsilyl)methyl substituents (Figure 6). While we observe the lowest energy transition for [(Me3Si)3Si]2(SiMe2)2 at 256 nm, the respective band for 8 displays a bathochromic shift of 11 nm to 267 nm. The absorption maximum for 17, which is a hybrid between 8 and the parent compound containing only one (trimethylsilyl)methyl group, lies expectedly at 262 nm. When the spacer between the branched units is increased by another dimethylsilylene unit, the comparison between the low-energy absorptions of [(Me3Si)3Si]2(SiMe2)3 (269 nm) and 9 (276 nm) shows only a bathochromic shift of 7 nm. On going a step further with an octamethyltetasilanylene spacer, the absorption bands of [(Me3Si)3Si]2(SiMe2)4 (280 nm) and 10 (284 nm) are as close as 4 nm.

Figure 6.

Figure 6

Open in a new tab

Comparison of UV absorption spectra of bis[tris(trimethylsilyl)silyl]-substituted permethyloligosilanes with those of the respective (trimethylsilyl)methyl derivatives 8–11 and 17.

The UV spectrum of [(Me3Si)3Si]2(SiMe2)6 displays two bands in the low-energy region (295/279 nm), which can be attributed to two conformations.16,19 The absorption at 295 nm corresponds to the transoid-aligned decasilane conformer, whereas the conformer which absorbs at 279 nm contains a transoid-aligned octasilane segment. The situation for compound 11 is quite similar. Two absorption bands are observed (293/283 nm) which are nearly identical with those of [(Me3Si)3Si]2(SiMe2)6. As could be expected from the trend described above, an increase of the spacer lengths by another two dimethylsilylene units further diminishes the influence of the (trimethylsilyl)methyl units. The absorption intensities of the two bands of [(Me3Si)3Si]2(SiMe2)6 are different, with the lower energy band being stronger, indicating that the aligned decasilane unit exists in a greater proportion. In contrast to this, we observe nearly identical absorption intensities for the two bands of 11, hinting at similar numbers of transoid-aligned octasilane and decasilane conformers. This difference between [(Me3Si)3Si]2(SiMe2)6 and 11 clearly points at a diminished steric influence of the (Me3Si)2(Me3SiCH2)Si group compared to the (Me3Si)3Si unit. As a final observation, it may also be worth mentioning that the absorption intensities of substances of the type [(Me3Si)3Si]2(SiMe2)n are substantially higher than those of compounds 9–11. The reason for this is not quite clear yet but may be connected to the fact that rotation of the (Me3Si)2(Me3SiCH2)Si group yields only two out of three conformers with all-transoid σ-bond conjugation.

Conclusion

α,ω-Bis[tris(trimethylsilyl)silyl]-substituted methylated oligosilanes were shown to exhibit a strong tendency to engage in all-transoid conformations.(19) Upon the replacement of one or two terminal trimethylsilyl by (trimethylsilyl)methyl groups in these compounds, the conformational properties were not shown to change much. Nevertheless, a comparison of the two types of compounds did show some interesting details (Table 1). The most pronounced differences are between [(Me3Si)3Si]2(SiMe2)2 and compound 8. The low-energy absorption maximum of 8 is red-shifted 11 nm. In addition the crystal structure of 8 does not exhibit the expected all-transoid conformation but features a torsion angle around the central Si–Si bond of 128°. This is unusual, as it clearly points at a much higher flexibility of the main chain. The bathochromically shifted absorption maximum indicates that in solution a strong preference still exists for an all-transoid orientation. With increasing spacer lengths the differences with respect to both solid-state behavior and absorption properties become smaller. For compound 11, with a hexasilanylene spacer, clearly the bulk of the end groups is no longer sufficient to make the all-transoid conformation the preferred one in solution.

Table 1. Comparison of Low-Energy Absorption Maxima (nm) and Dihedral Angles (deg) of Main Chains Derived from the Crystal Structures of 8–11 and 17 with Those of the Respective (Me3Si)3Si-Terminated Compounds.

compd λmax ω1 ω2 ω3 ω4 ω5 ω6 ω7 conformation
[(Me3Si)3Si]2(SiMe2)2 256 159 180 159         TAT
8 267 166 128 156         TET
17 262                
[(Me3Si)3Si]2(SiMe2)3 269 161 160 167 164       TTTT
9 276 157/159a 165/157a 160/159a 174/171a       TTTT
[(Me3Si)3Si]2(SiMe2)4 280 162 159 180 159 162     TTATT
10 284 158 158 180 158 158     TTATT
[(Me3Si)3Si]2(SiMe2)6 295/279 161 168 161 155 167 164 164 TTTTTTT
11 293/283                
Open in a new tab
a

two molecules in the asymmetric unit.

Experimental Section

General Remarks

All reactions involving air-sensitive compounds were carried out under an atmosphere of nitrogen or argon using either Schlenk techniques or a glovebox. Solvents were dried using a column solvent purification system.(34) Potassium tert-butoxide was purchased from Merck. All other chemicals were used as received from chemical suppliers.

Aqueous workup was performed by pouring the reaction mixture into 2 M H2SO4, followed by separation of the layers. Subsequently the aqueous phase was extracted twice. The combined organic extracts were washed with a saturated aqueous sodium hydrogen carbonate solution and then dried over sodium sulfate.

1H (300 MHz), 13C (75.4 MHz), and 29Si (59.3 MHz) NMR spectra were recorded on a Varian Unity INOVA 300 spectrometer. If not noted otherwise, C6D6 was used as solvent for all samples. To compensate for the low isotopic abundance of 29Si, the INEPT pulse sequence was used for the amplification of the signal.35,36

Elemental analyses were done using a Heraeus Vario Elementar EL apparatus. Analysis values for carbon show values that are consistently too low, which is attributed to the formation and incomplete combustion of silicon carbide. Lengthening the combustion times could be used to obtain slightly improved values.

GC analyses were carried out on an HP 5890 series II instrument equipped with an HP-1 ms capillary column (25 m × 0.251 mm; 0.33 μm) and an HP 5971 mass spectrometer. UV–vis absorption spectra were recorded on a Perkin–Elmer Lambda 35 spectrometer in pentane solution. QtiPlot was used for analysis and plotting of the spectra.(37)

For X-ray structure analyses crystals were mounted onto the tips of glass fibers, and data collection was performed with a Bruker-AXS SMART APEX CCD diffractometer using graphite-monochromated Mo Kα radiation (0.710 73 Å). The data were reduced to Fo2 and corrected for absorption effects with SAINT(38) and SADABS,39,40 respectively. The structures were solved by direct methods and refined by full-matrix least-squares methods (SHELXL97).(41) If not noted otherwise, all non-hydrogen atoms were refined with anisotropic displacement parameters.

Crystallographic data (excluding structure factors) for the structures of compounds 7–10 and 12 reported in this paper (Table 2) have been deposited with the Cambridge Crystallographic Data Center as Supplementary Publication Nos. CCDC-670861 (7), -670859 (8), -793979 (9), -670863 (10), and -670860 (12). Copies of the data can be obtained free of charge at http://www.ccdc.cam.ac.uk/products/csd/request/.

Table 2. Crystallographic Data for Compounds 7–10 and 12.

  7 8 9 10 12
empirical formula Si8C20H58 Si10C24H70 Si22C524H152 Si12C28H82 Si8C22H62
Mw 523.38 639.70 1395.72 756.02 551.44
temp (K) 100(2) 100(2) 100(2) 100(2) 100(2)
size (mm) 0.40 × 0.30 × 0.20 0.50 × 0.40 × 0.25 0.35 × 0.24 × 0.16 0.34 × 0.26 × 0.20 0.45 × 0.36 × 0.30
cryst syst triclinic triclinic monoclinic monoclinic monoclinic
space group P1̅ P1̅ P21/c P21/n C2/c
a (Å) 9.5214(2) 10.918(2) 19.020(4) 8.0514(2) 15.188(3)
b (Å) 9.955(2) 13.549(3) 16.414(3) 32.411(7) 9.960(2)
c (Å) 10.396(2) 15.158(3) 29.778(6) 9.924(2) 25.704(5)
α (deg) 93.09(3) 79.34(3) 90 90 90
β (deg) 111.65(3) 77.65(3) 99.97(3) 111.07(3) 103.36(3)
γ (deg) 107.06(3) 75.41 90 90 90
V (Å3) 860.9(3) 2099.3(7) 9156(3) 2416.4(8) 3783.1(2)
Z 1 2 4 2 4
ρcalcd (g cm–3) 1.010 1.012 1.012 1.039 0.968
abs coeff (mm–1) 0.319 0.326 0.328 0.339 0.293
F(000) 290 708 3088 836 1224
θ range (deg) 2.14 < θ < 26.31 1.39 < θ < 24.00 1.09 < θ < 25.00 2.29 < θ < 26.38 1.63 < θ < 23.50
no. of collected/unique rflns 6877/3450 13 941/6580 64 873/16 131 18 871/4935 11 475/2791
completeness to θ (%) 98.5 99.5 100 99.8 100
no. of data/restraints/params 3450/0/136 6580/0/329 16 131/150/851 4935/0/194 2791/0/145
goodness of fit on F2 1.24 1.26 1.14 1.11 1.35
final R indices (I > 2σ(I)) R1 = 0.056, wR2 = 0.116 R1 = 0.092, wR2 = 0.183 R1 = 0.100, wR2 = 0.178 R1 = 0.060, wR2 = 0.116 R1 = 0.093, wR2 = 0.198
R indices (all data) R1 = 0.063, wR2 = 0.119 R1 = 0.112, wR2 = 0.191 R1 = 0.148, wR2 = 0.199 R1 = 0.081, wR2 = 0.124 R1 = 0.099, wR2 = 0.201
largest diff peak/hole (e/Å3) 0.51/–0.28 0.77/–0.49 0.70/–0.46 0.50/–0.34 0.91/–0.42
Open in a new tab

Tris(trimethylsilyl)silylpotassium (1),(23) 1,4-bis[tris(trimethylsilyl)silyl]butane (12),(42) dichlorotetramethyldisilane,(43) 1,3-dibromohexamethyltrisilane,(44) 1,4-dichlorooctamethyltetrasilane,(45) 1,1,1,8,8,8-hexakis(trimethylsilyl)dodecamethyloctasilane,(16) chloropentamethyldisilane,(46) and 1,1,1,4,4,4-hexakis(trimethylsilyl)-2,2,3,3-tetramethyltetrasilane24,25 were prepared and have spectral properties in accord with those published.

Tris(trimethylsilyl)[(trimethylsilyl)methyl]silane (2)

At 0 °C a suspension of 1 (2.08 g, 3.78 mmol) in benzene (20 mL) was added slowly to chloromethyltrimethylsilane (0.464 g, 3.78 mmol) in benzene (20 mL). The reaction mixture remained colorless during the whole addition process, and a white precipitate was formed. After 2 h at 0 °C the suspension was warmed to room temperature followed by an aqueous workup (diethyl ether). A colorless viscous liquid of 2 (1.19 g, 94%) was obtained. 1H NMR (δ, ppm): 0.24 (s, 27H, Me3Si), 0.11 (s, 9H, Me3Si), −0.10 (s, 2H, CH2). 13C NMR (δ, ppm): 1.6 (Me3SiCH2), 1.3 (Me3Si), −8.3 (CH2). 29Si NMR (δ, ppm): 1.8 (Me3SiCH2), −12.9 (Me3Si), −85.1 (Me3SiSi). MS (70 eV; m/z (%)): 334 (5.5) [M+], 261 (23.9) [M+ – SiMe3], 231 (8.3) [M+ – SiMe5], 187 (89.0) [M+ – Si2Me6H], 131 (14.1) [Si2Me5+], 73 (100) [SiMe3+]. Anal. Calcd for C13H38Si5 (334.87 g/mol): C, 46.63; H, 11.44. Found: C, 46.87; H, 11.25. UV absorption: λ1 211 nm (ε1 = 1.2 × 104 M–1 cm–1).

[Bis(trimethylsilyl)((trimethylsilyl)methyl)silyl]potassium–18-crown-6 (3)

Compound 2 (9.13 g, 27.3 mmol), KOtBu (3.102 g, 27.3 mmol), and 18-crown-6 (7.30 g, 27.3 mmol) were dissolved in benzene (50 mL). The cleavage reaction proceeded within 4 h and yielded 3 as a red solution. 1H NMR (δ, ppm): 3.20 (s, 24H, 18-crown-6), 0.51 (s, 18H, Me3Si), 0.32 (s, 9H, Me3Si), 0.24 (s, 2H, CH2). 13C NMR (δ, ppm): 69.9 (18-crown-6), 4.5 (Me3Si), 1.7 (Me3SiCH2), −7.5 (CH2). 29Si NMR (δ, ppm): 0.8 (Me3SiCH2), −6.6 (Me3Si), −128.6 (Me3SiSi).

Bis(trimethylsilyl)bis((trimethylsilyl)methyl)silane (4)

The same procedure as described for 2 was used, with 3 (2.37 mmol) and chloromethyltrimethylsilane (0.291 g, 2.37 mmol). A colorless viscous liquid of 4 (0.743 g, 90%) was obtained. 1H NMR (δ, ppm): 0.22 (s, 18H, Me3Si), 0.13 (s, 18H, Me3SiCH2), −0.01 (s, 4H, CH2). 13C NMR (δ, ppm): 2.1 (Me3Si), −0.1 (Me3SiCH2), −1.6 (CH2). 29Si NMR (δ, ppm): 1.2 (Me3SiCH2), −16.7 (Me3Si), −43.9 (Me3SiSi). MS (70 eV; m/z (%)): 348 (0.6) [M+], 275 (6.1) [M+ – SiMe3], 245 (2.8) [M+ – SiMe5], 187 (100) [M+ – Si2Me7], 131 (22.3) [Si2Me5+], 73 (52.0) [SiMe3+]. Anal. Calcd for C14H40Si5 (348.89 g/mol): C, 48.19; H, 11.56. Found: C, 48.16; H, 11.45. UV absorption: λ1 208 nm (ε1 = 5.5 × 103 M–1 cm–1), λ2 222 nm (ε2 = 7.1 × 103 M–1 cm–1).

[Bis((trimethylsilyl)methyl)(trimethylsilyl)silyl]potassium–18-crown-6 (5)

The same procedure as described for 3 was used, with 4 (7.82 g, 22.5 mmol), KOtBu (2.52 g, 22.5 mmol), and 18-crown-6 (5.94 g, 22.5 mmol). 1H NMR (δ, ppm): 3.19 (s, 24H, 18-crown-6), 0.25 (s, 9H, Me3Si), 0.22 (s, 18H, Me3SiCH2), −0.04 (s, 4H, CH2). 13C NMR (δ, ppm): 69.9 (18-crown-6), 2.5 (Me3Si), 1.0 (Me3SiCH2), −1.5 (CH2).29Si NMR (δ, ppm): 0.0 (Me3SiCH2), −12.0 (Me3Si), −66.5 (Me3SiSi).

Tris[(trimethylsilyl)methyl](trimethylsilyl)silane (6)

The same procedure as described for 2 was used, with 5 (0.792 g, 1.361 mmol) and chloromethyltrimethylsilane (0.167 g, 1.361 mmol). A colorless viscous liquid of 6 (0.403 g, 81%) was obtained. 1H NMR (δ, ppm): 0.21 (s, 9H, Me3Si), 0.14 (s, 27H, Me3SiCH2), 0.03 (s, 6H, CH2). 13C NMR (δ, ppm): 4.3 (Me3Si), 2.2 (Me3SiCH2), −0.8 (CH2). 29Si NMR (δ, ppm): 0.2 (Me3SiCH2), −15.9 (Me3Si), −20.2 (Me3SiSi). MS (70 eV; m/z (%)): 362 (0.3) [M+], 289 (3.0) [M+ – SiMe3], 259 (1.0) [M+ – SiMe5], 201 (100) [M+ – Si2Me7], 73 (40.7) [SiMe3+]. Anal. Calcd for C15H42Si5 (362.92 g/mol): C, 49.64, H, 11.66. Found: C, 49.56; H, 11.49. UV absorption: λ1 198 nm (ε1 = 1.6 × 104 M–1 cm–1), shoulder at λ2 221 nm (ε2 = 1.8 × 103 M–1 cm–1).

1,1,2,2-Tetrakis(trimethylsilyl)-1,2-bis[(trimethylsilyl)methyl]disilane (7)

A procedure similar to that described for 2 was used, with 3 (1.91 mmol) and dibromoethane (0.179 g, 0.955 mmol) in 150 mL of diethyl ether. The reaction was carried out at −78 °C instead of 0 °C. Compound 7 (0.473 g, 95%) was obtained as a colorless crystalline solid (mp 48–51 °C). 1H NMR (δ, ppm): 0.35 (s, 36H, Me3Si), 0.17 (s, 4H, Me3SiCH2), 0.15 (s, 18H, Me3SiCH2). 13C NMR (δ, ppm): 2.9 (Me3Si), 1.9 (Me3SiCH2), −1.6 (CH2). 29Si NMR (δ, ppm): 1.3 (Me3SiCH2), −12.8 (Me3Si), −72.6 (Me3SiSi). MS (70 eV; m/z (%)): 522 (0.9) [M+], 449 (1.3) [M+ – SiMe3], 362 (1.4) [M+ – Si2Me6CH2], 347 (4.8) [M+ – Si2Me7CH2], 289 (4.5) [Si5Me9CH2+], 261 (36.8) [Si4Me9CH2+], 246 (80.9) [Si4Me8CH2+], 187 (88.8) [Si3Me6CH2+], 173 (33.5) [Si3Me5CH2+], 131 (14.1) [Si2Me5+], 73 (100) [SiMe3+]. Anal. Calcd for C20H58Si8 (523.36 g/mol): C, 45.90, H, 11.17. Found: C, 45.41; H, 11.08. UV absorption: λ1 211 nm (ε1 = 5.2 × 104 M–1 cm–1), shoulders at λ2 230 nm and λ3 245 nm.

1,1,4,4-Tetrakis(trimethylsilyl)-1,4-bis[(trimethylsilyl)methyl]tetramethyltetrasilane (8)

A procedure similar to that described for 2 was used, with 3 (1.60 mmol) and 1,2-dichlorotetramethyldisilane (0.150 g, 0.801 mmol). Compound 8 (0.490 g, 96%) was obtained as a colorless crystalline solid (mp 56–59 °C). 1H NMR (δ, ppm): 0.45 (s, 12H, Me2Si), 0.28 (s, 36H, Me3Si), 0.13 (s, 18H, Me3SiCH2), 0.03 (s, 4H, CH2). 13C NMR (δ, ppm): 2.3 (Me3Si), 1.9 (Me3SiCH2), −0.2 (Me2Si), −6.1 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −12.6 (Me3Si), −32.5 (Me2Si), −77.7 (Me3SiSi). MS (70 eV; m/z (%)): 638 (2.0) [M+], 377 (17.4) [Si6Me13CH2+], 319 (18.9) [Si5Me11CH2+], 304 (18.3) [Si5Me10CH2+], 232 (24.6) [Si4Me8+], 131 (39.5) [Si2Me5+], 73 (100) [SiMe3+]. Anal. Calcd for C24H70Si10 (639.67 g/mol): C, 45.06; H, 11.03. Found: C, 44.88; H, 10.95. UV absorption: λ1 210 nm (ε1 = 3.9 × 104 M–1 cm–1), λ2 267 nm (ε2 = 4.2 × 104 M–1 cm–1).

1,1,5,5-Tetrakis(trimethylsilyl)-1,5-bis[(trimethylsilyl)methyl]hexamethylpentasilane (9)

A procedure similar to that described for 2 was used, with 3 (3.27 mmol) and 1,3-dibromohexamethyltrisilane (0.545 g, 1.63 mmol). Compound 9 (1.08 g, 95%) was obtained as a colorless crystalline solid (mp 65–68 °C). 1H NMR (δ, ppm): 0.50 (s, 6H, Me2Si), 0.48 (s, 12H, Me2Si), 0.32 (s, 36H, Me3Si), 0.16 (s, 18H, Me3SiCH2), 0.08 (s, 4H, CH2). 13C NMR (δ, ppm): 2.1 (Me3Si), 1.8 (Me3SiCH2), −0.8 (Me2Si), −2.0 (Me2Si), −6.1 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −12.6 (Me3Si), −32.9 (Me2Si), −35.8 (Me2Si), −78.0 (Me3SiSi). Anal. Calcd for C26H76Si11 (697.82 g/mol): C, 44.75; H, 10.98. Found: C, 45.11; H, 11.02. UV absorption: λ1 211 nm (ε1 = 3.4 × 104 M–1 cm–1), shoulder at λ2 256 nm, λ3 276 nm (ε3 = 3.3 × 104 M–1 cm–1).

1,1,6,6-Tetrakis(trimethylsilyl)-1,6-bis[(trimethylsilyl)methyl]octamethylhexasilane (10)

A procedure similar to that described for 2 was used, with 3 (0.509 g, 0.901 mmol) and 1,4-dichlorooctamethyltetrasilane (0.136 g, 0.451 mmol). Compound 10 (0.313 g, 92%) was obtained as a colorless crystalline solid (mp 167–169 °C). 1H NMR (δ, ppm): 0.47 (s, 12H, Me2Si), 0.45 (s, 12H, Me2Si), 0.32 (s, 36H, Me3Si), 0.16 (s, 18H, Me3SiCH2), 0.17 (s, 4H, CH2). 13C NMR (δ, ppm): 2.1 (Me3Si), 1.8 (Me3SiCH2), −0.7 (Me2Si), −2.8 (Me2Si), −6.2 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −12.6 (Me3Si), −33.6 (Me2Si), −35.8 (Me2Si), −78.0 (Me3SiSi). Anal. Calcd for C28H82Si12 (755.98 g/mol): C, 44.49; H, 10.93. Found: C, 44.62; H, 10.93. UV absorption: λ1 209 nm (ε1 = 4.6 × 104 M–1 cm–1), λ2 284 nm (ε2 = 4.9 × 104 M–1 cm–1).

1,1,8,8-Tetrakis(trimethylsilyl)-1,8-bis[(trimethylsilyl)methyl]dodecamethyloctasilane (11)

The dianion derived from 1,1,1,8,8,8-hexakis(trimethylsilyl)-dodecamethyloctasilane was prepared according to the procedure described for 3 using the octasilane (0.311 g, 0.368 mmol), KOtBu (83 mg, 0.74 mmol), and 18-crown-6 (196 mg, 0.74 mmol). The reaction of the dianion was done according to a procedure similar to that described for 2 using chloromethyltrimethylsilane (91 mg, 2 equiv). Compound 11 (290 mg, 90%) was obtained as a colorless crystalline solid (mp 70–75 °C) after recrystallization (Et2O/isopropyl alcohol). 1H NMR (δ, ppm): 0.47 (s, 12H, Me2Si), 0.44 (s, 12H, Me2Si), 0.40 (s, 12H, Me2Si), 0.32 (s, 36H, Me3Si), 0.17 (s, 18H, Me3SiCH2), 0.08 (s, 4H, CH2). 13C NMR (δ, ppm): 2.1 (Me3Si), 1.8 (Me3SiCH2), −0.8 (Me2Si), −2.8 (Me2Si), −3.4 (Me2Si), −6.2 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −12.6 (Me3Si), −33.8 (Me2Si), −36.3 (Me2Si), −36.5 (Me2Si), −78.4 (Me3SiSi). Anal. Calcd for C32H94Si14 (872.29 g/mol): C, 44.06; H, 10.86. Found: C, 43.73; H, 10.83. UV absorption: λ1 210 nm (ε1 = 5.5 × 104 M–1 cm–1), λ2 = 283 nm (ε2 = 4.4 × 104 M–1 cm–1), λ3 293 nm (ε3 = 4.2 × 104 M–1 cm–1).

1,4-Bis[tris(trimethylsilyl)silyl]butane (12)

1 (1.09 mmol) in THF (10 mL) was added slowly to a stirred solution of 1,4-ditosylbutane (0.56 mmol, 223 mg) in THF (10 mL). After 12 h at room temperature, the reaction mixture was subjected to an aqueous workup (diethyl ether). Compound 12 (258 mg, 88%) was obtained as a colorless crystalline solid (mp 165–166 °C). 1H NMR (δ, ppm): 1.68 (m, 4H), 1.02 (m, 4H), 0.25 (s, 54H). 13C NMR (δ, ppm): 34.4 (SiCH2CH2), 7.6 (SiCH2), 1.3 (Me3Si). 29Si NMR (δ, ppm): −13.1 (Me3Si), −81.9 (Me3SiSi). Anal. Calcd for C22H62Si8 (551.41 g/mol): C, 47.92; H, 11.33. Found: C, 48.08; H, 11.60. UV absorption: λ1 211 nm (ε1 = 1.6 × 104 M–1 cm–1), shoulder at λ2 228 nm (ε2 = 5.2 × 103 M–1 cm–1).

1,1-Bis(trimethylsilyl)-1-[(trimethylsilyl)methyl]pentamethyltrisilane (13)

A procedure similar to that described for 2 was used, with 3 (1.07 mmol) and chloropentamethyldisilane (0.179 g, 1.07 mmol). Instead of benzene THF was used, and no 18-crown-6 was required. Compound 13 (330 mg, 78%) was obtained as a colorless liquid. 1H NMR (δ, ppm): 0.28 (s, 6H, Me2Si), 0.25 (s, 18H, Me3Si), 0.17 (s, 9H, Me3Si), 0.10 (s, 9H, Me3Si), −0.05 (s, 2H, CH2). 13C NMR (δ, ppm): 1.9 (Me3Si), 1.8 (Me3Si), 0.6 (Me3Si), −2.7 (Me2Si), −6.7 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −12.3 (Me3Si), −14.7 (Me3Si), −40.7 (Me2Si), −80.8 (Me3SiSi). Anal. Calcd for C15H44Si6 (393.02 g/mol): C, 45.84; H, 11.28. Found: C, 46.19; H, 11.28. UV absorption: λ1 215 nm (ε1 = 1.3 × 104 M–1 cm–1), λ2 227 nm (ε2 = 1.1 × 104 M–1 cm–1).

1,1,1,2,2-Pentakis(trimethylsilyl)-2-bis[(trimethylsilyl)methyl]disilane (14)

Similar procedure as described for 13 starting from hexakis(trimethylsilyl)disilane (345 mg, 0.696 mmol) and KOtBu (79 mg, 0.70 mmol) followed by addition to chloromethyltrimethylsilane (86 mg, 0.70 mmol). Compound 14 (290 mg, 82%) was obtained as a colorless crystalline solid (mp: decomposition at 180 °C). 1H NMR (δ, ppm): 0.32 (s, 27H, Me3Si), 0.31 (s, 18H, Me3Si), 0.12 (s, 9H, Me3Si), 0.09 (s, 2H, CH2). 13C NMR (δ, ppm): 4.3 (Me3Si), 3.0 (Me3Si), 2.0 (Me3Si), 0.1 (CH2). 29Si NMR (δ, ppm): 1.2 (Me3SiCH2), −9.9 (Me3Si), −13.3 (Me3Si), −71.2 (Me2Si), −123.0 (Me3SiSi). Anal. Calcd for C19H56Si8 (509.33 g/mol): C, 44.80; H, 11.08. Found: C, 44.60; H, 11.01. UV absorption: λ1 216 nm (ε1 = 2.3 × 104 M–1 cm–1).

1,1,2,2-Tetrakis(trimethylsilyl)-1-bis[(trimethylsilyl)methyl]-2-methyldisilane (15)

A procedure similar to that described for 2 was used, starting with 14 (406 mg, 0.797 mmol) and KOtBu (89 mg, 0.80 mmol) followed by addition to dimethyl sulfate (101 mg, 1.01 equiv). Instead of benzene THF was used, and no 18-crown-6 was required. Compound 15 (315 mg, 88%) was obtained as a colorless oil. 1H NMR (δ, ppm): 0.32 (s, 3H, MeSi), 0.30 (s, 18H, Me3Si), 0.27 (s, 18H, Me3Si), 0.19 (s, 2H, CH2), 0.14 (s, 9H, Me3Si). 13C NMR (δ, ppm): 2.3 (Me3Si), 1.9 (Me3Si), 1.7 (Me3Si), 0.4 (MeSi), −8.5 (CH2). 29Si NMR (δ, ppm): 1.4 (Me3SiCH2), −11.8 (Me3Si), −12.8 (Me3Si), −76.1 (Me3SiSi), −78.1 (Me3SiSi). Anal. Calcd for C17H50Si7 (451.18 g/mol): C, 45.26; H, 11.17. Found: C, 45.26; H, 10.75. UV absorption: λ1 216 nm (ε1 = 1.4 × 104 M–1 cm–1).

1,1,2,2-Tetrakis(trimethylsilyl)-1-[(trimethylsilyl)methyl]pentamethyltetrasilane (16)

A procedure similar to that described for 13 was used, starting with 14 (696 mg, 1.366 mmol) and KOtBu (153 mg, 1.36 mmol) followed by addition to chloropentamethyldisilane (228 mg, 1.36 mmol). Compound 16 (720 mg, 93%) was obtained as a colorless crystalline solid (mp: 130–140 °C). 1H NMR (δ, ppm): 0.39 (s, 6H, Me2Si), 0.35 (s, 18H, Me3Si), 0.33 (s, 18H, Me3Si), 0.20 (s, 9H, Me3Si), 0.14 (s, 9H, Me3Si), 0.09 (s, 2H, CH2). 29Si NMR (δ, ppm): 1.2 (Me3SiCH2), −10.0 (Me3Si), −13.1 (Me3Si), −13.2 (Me3Si), −38.2 (Me2Si), −69.7 (Me3SiSi), −115.2 (Me3SiSi). Anal. Calcd for C21H62Si9 (567.49 g/mol): C, 44.45; H, 11.01. Found: C, 44.46; H, 10.83. UV absorption: λ1 216 nm (ε1 = 1.9 × 104 M–1 cm–1).

1,1,1,4,4-Pentakis(trimethylsilyl)-4-[(trimethylsilyl)methyl]tetramethyltetrasilane (17)

A procedure similar to that described for 2 was used, starting with 1,1,1,4,4,4-hexakis(trimethylsilyl)-tetramethyltetrasilane (391 mg, 0.639 mmol), 18-crown-6 (169 mg, 0.639 mmol), and KOtBu (72 mg, 0.639 mmol) followed by addition to chloromethyltrimethylsilane (79 mg, 1.01 equiv). Compound 17 (360 mg, 90%) was obtained as a colorless crystalline solid (mp: 203–206 °C). 1H NMR (δ, ppm): 0.54 (s, 6H, Me2Si), 0.49 (s, 6H, Me2Si), 0.33 (s, 27H, Me3Si), 0.31 (s, 18H, Me3Si), 0.15 (s, 9H, Me3Si), 0.07 (s, 2H, CH2). 13C NMR (δ, ppm): 3.6 (Me3Si), 2.3 (Me3Si), 1.8 (Me3SiCH2), 1.6 (Me2Si), −0.3 (Me2Si), −6.0 (CH2). 29Si NMR (δ, ppm): 1.6 (Me3SiCH2), −9.7 (Me3Si), −12.6 (Me3Si), −29.8 (Me2Si), −32.7 (Me2Si), −77.5 (Me3SiSi), −128.3 (Me3SiSi). Anal. Calcd for C23H68Si10 (625.64 g/mol): C, 44.15; H, 10.96. Found: C, 43.74; H, 10.87. UV absorption: λ1 215 nm (ε1 = 2.4 × 104 M–1 cm–1), λ2 262 nm (ε2 = 3.1 × 103 M–1 cm–1).

Acknowledgments

This study was supported by the Austrian Fonds zur Förderung der wissenschaftlichen Forschung (FWF) via the projects Y-120 and P-18538.

Supporting Information Available

CIF files giving X-ray crystallographic data for 7–10 and 12. This material is available free of charge via the Internet at http://pubs.acs.org.

Supplementary Material

om1011159_si_001.cif (102.6KB, cif)

References

  1. Miller R. D.; Michl J. Chem. Rev. 1989, 89, 1359–1410. [Google Scholar]
  2. Fukazawa A.; Tsuji H.; Tamao K. J. Am. Chem. Soc. 2006, 128, 6800–6801. [DOI] [PubMed] [Google Scholar]
  3. Mallesha H.; Tsuji H.; Tamao K. Organometallics 2004, 23, 1639–1642. [Google Scholar]
  4. Tamao K.; Tsuji H.; Terada M.; Asahara M.; Yamaguchi S.; Toshimitsu A. Angew. Chem., Int. Ed. 2000, 39, 3287–3290. [PubMed] [Google Scholar]
  5. Tsuji H.; Terada M.; Toshimitsu A.; Tamao K. J. Am. Chem. Soc. 2003, 125, 7486–7487. [DOI] [PubMed] [Google Scholar]
  6. Tsuji H.; Michl J.; Tamao K. J. Organomet. Chem. 2003, 685, 9–14. [Google Scholar]
  7. Tsuji H.; Fukazawa A.; Yamaguchi S.; Toshimitsu A.; Tamao K. Organometallics 2004, 23, 3375–3377. [Google Scholar]
  8. Bande A.; Michl J. Chem. Eur. J. 2009, 15, 8504–8517. [DOI] [PubMed] [Google Scholar]
  9. Lambert J. B.; Pflug J. L.; Stern C. L. Angew. Chem., Int. Ed. Engl. 1995, 34, 98–99. [Google Scholar]
  10. Lambert J. B.; Liu X.; Wu H.; Pflug J. L. J. Chem. Soc., Perkin Trans. 2 1999, 2747–2749. [Google Scholar]
  11. Lambert J. B.; Wu H. Organometallics 1998, 17, 4904–4909. [Google Scholar]
  12. Lambert J. B.; Wu H. Magn. Reson. Chem. 2000, 38, 388–389. [Google Scholar]
  13. Nanjo M.; Sunaga T.; Sekiguchi A.; Horn E. Inorg. Chem. Commun. 1999, 2, 203–206. [Google Scholar]
  14. Sekiguchi A.; Nanjo M.; Kabuto C.; Sakurai H. J. Am. Chem. Soc. 1995, 117, 4195–4196. [Google Scholar]
  15. Baumgartner J.; Frank D.; Kayser C.; Marschner C. Organometallics 2005, 24, 750–761. [Google Scholar]
  16. Wallner A.; Wagner H.; Baumgartner J.; Marschner C.; Rohm H. W.; Köckerling M.; Krempner C. Organometallics 2008, 27, 5221–5229. [Google Scholar]
  17. Baumgartner J.; Fischer R.; Fischer J.; Wallner A.; Marschner C.; Flörke U. Organometallics 2005, 24, 6450–6457. [Google Scholar]
  18. Krempner C.; Köckerling M. Organometallics 2008, 27, 346–352. [Google Scholar]
  19. Marschner C.; Baumgartner J.; Wallner A. Dalton Trans. 2006, 5667–5674. [DOI] [PubMed] [Google Scholar]
  20. Wallner A.; Hölbling M.; Baumgartner J.; Marschner C. Silicon Chem. 2006, 3, 175–185. [Google Scholar]
  21. Berkefeld A.; Troegel D.; Burschka C.; Tacke R. Organometallics 2010, 4548–4554. [Google Scholar]
  22. Wagner H.; Baumgartner J.; Marschner C.; Poelt P.. Organometallics 2011, DOI 10.1021/om1011165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Marschner C. Eur. J. Inorg. Chem. 1998, 1998, 221–226. [Google Scholar]
  24. Whittaker S. M.; Brun M.; Cervantes-Lee F.; Pannell K. H. J. Organomet. Chem. 1995, 499, 247–252. [Google Scholar]
  25. Fischer R.; Frank D.; Gaderbauer W.; Kayser C.; Mechtler C.; Baumgartner J.; Marschner C. Organometallics 2003, 22, 3723–3731. [Google Scholar]
  26. Bock H.; Meuret J.; Ruppert K. Angew. Chem. 1993, 105, 413–415. [Google Scholar]
  27. Fronczek F. R.; Lickiss P. D. Acta Crystallogr., Sect. C 1993, 49, 331–333. [Google Scholar]
  28. Mallela S. P.; Bernal I.; Geanangel R. A. Inorg. Chem. 1992, 31, 1626–1627. [Google Scholar]
  29. Bock H.; Meuret J.; Ruppert K. J. Organomet. Chem. 1993, 445, 19–28. [Google Scholar]
  30. Lambert J. B.; Pflug J. L.; Allgeier A. M.; Campbell D. J.; Higgins T. B.; Singewald E. T.; Stern C. L. Acta Crystallogr., Sect. C 1995, 51, 713–715. [Google Scholar]
  31. Gross T.; Oehme H.; Kempe R. Organometallics 1999, 18, 1815–1817. [Google Scholar]
  32. Blanton J. R.; Diminnie J. B.; Chen T.; Wiltz A. M.; Xue Z. Organometallics 2001, 20, 5542–5546. [Google Scholar]
  33. Kumada M.; Tamao K. Adv. Organomet. Chem. 1968, 6, 19–117. [Google Scholar]
  34. Pangborn A. B.; Giardello M. A.; Grubbs R. H.; Rosen R. K.; Timmers F. J. Organometallics 1996, 15, 1518–1520. [Google Scholar]
  35. Morris G. A.; Freeman R. J. Am. Chem. Soc. 1979, 101, 760–762. [Google Scholar]
  36. Helmer B. J.; West R. Organometallics 1982, 1, 877–879. [Google Scholar]
  37. http://soft.proindependent.com/qtiplot.html.
  38. SAINTPLUS: Software Reference Manual, Version 6.45; Bruker-AXS: Madison, WI, 1997–2003. [Google Scholar]
  39. Sheldrick G. M.SADABS, Version 2.10; Bruker AXS Inc., Madison, WI, 2003.
  40. Blessing R. H. Acta Crystallogr., Sect. A 1995, 51, 33–38. [DOI] [PubMed] [Google Scholar]
  41. Sheldrick G. M. Acta Crystallogr., Sect. A 2007, 64, 112–122. [DOI] [PubMed] [Google Scholar]
  42. Mechtler C.; Marschner C. Tetrahedron Lett. 1999, 40, 7777–7778. [Google Scholar]
  43. Hengge E.; Waldhör S. Monatsh. Chem. 1974, 105, 671–683. [Google Scholar]
  44. Middlecamp C.; Wojnowski W.; West R. J. Organomet. Chem. 1977, 140, 133–143. [Google Scholar]
  45. Gilman H.; Inoue S. J. Org. Chem. 1964, 29, 3418–3419. [Google Scholar]
  46. Ishikawa M.; Kumada M.; Sakurai H. J. Organomet. Chem. 1970, 23, 63–69. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

om1011159_si_001.cif (102.6KB, cif)

Articles from Organometallics are provided here courtesy of American Chemical Society

RESOURCES