-
2
-
-
33751157886
-
-
Bartsch, M.; Bornhauser, P.; Calzaferri, G. J. Phys. Chem. 1994, 98, 2817-2831.
-
(1994)
J. Phys. Chem.
, vol.98
, pp. 2817-2831
-
-
Bartsch, M.1
Bornhauser, P.2
Calzaferri, G.3
-
3
-
-
0024622432
-
-
Feher F. J.; Newman, D. A.; Walzer, J. F. J. Am. Chem. Soc. 1989, 111, 1741-1748. Lichtenhan, J. D.; Vu, N. Q.; Carter, J. A.; Gilman, J. W.; Feher, F. J. Macromolecules 1993, 26, 2141-2142.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 1741-1748
-
-
Feher, F.J.1
Newman, D.A.2
Walzer, J.F.3
-
4
-
-
0000744644
-
-
Feher F. J.; Newman, D. A.; Walzer, J. F. J. Am. Chem. Soc. 1989, 111, 1741-1748. Lichtenhan, J. D.; Vu, N. Q.; Carter, J. A.; Gilman, J. W.; Feher, F. J. Macromolecules 1993, 26, 2141-2142.
-
(1993)
Macromolecules
, vol.26
, pp. 2141-2142
-
-
Lichtenhan, J.D.1
Vu, N.Q.2
Carter, J.A.3
Gilman, J.W.4
Feher, F.J.5
-
5
-
-
33845282181
-
-
Agaskar, P. A.; Day, V. W.; Klemperer, W. G. J. Am. Chem. Soc. 1987, 109, 5545.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 5545
-
-
Agaskar, P.A.1
Day, V.W.2
Klemperer, W.G.3
-
8
-
-
2542611109
-
-
(b) Lichtenhan, J. D.; Mantz, R. A.; Jones, P. F.; Carr, M. J. Am. Chem. Soc. Polym. Prprt. 1994, 35, 523-524.
-
(1994)
Am. Chem. Soc. Polym. Prprt.
, vol.35
, pp. 523-524
-
-
Lichtenhan, J.D.1
Mantz, R.A.2
Jones, P.F.3
Carr, M.J.4
-
10
-
-
26244438038
-
-
Jutzi, P.; Batz, C.; Mutluay, A. Z. Naturforsch. 1994, 49b, 1689-1692.
-
(1994)
Z. Naturforsch.
, vol.49 B
, pp. 1689-1692
-
-
Jutzi, P.1
Batz, C.2
Mutluay, A.3
-
17
-
-
85033815220
-
-
German Patent No. DE 3837397 A1, 1990
-
Weidner, R.; Zeller, N.; Deubzer, B.; Frey, V. German Patent No. DE 3837397 A1, 1990.
-
-
-
Weidner, R.1
Zeller, N.2
Deubzer, B.3
Frey, V.4
-
18
-
-
0020469181
-
-
(a) Bowen, R. L.; Cobb, E. N.; Rapson, J. E. J. Dent. Res. 1982, 61, 1070.
-
(1982)
J. Dent. Res.
, vol.61
, pp. 1070
-
-
Bowen, R.L.1
Cobb, E.N.2
Rapson, J.E.3
-
20
-
-
0023538170
-
-
(c) Tesoro, G. C.; Rajendran, G. P.; Park, C.; Uhlmann, D. R. J. Adhes. Sci. Technol. 1987, 1, 39.
-
(1987)
J. Adhes. Sci. Technol.
, vol.1
, pp. 39
-
-
Tesoro, G.C.1
Rajendran, G.P.2
Park, C.3
Uhlmann, D.R.4
-
22
-
-
84991968275
-
-
Harvey, D. F.; Lund, K. P.; Neil, D. A. J. Am. Chem. Soc. 1992, 114, 8424.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 8424
-
-
Harvey, D.F.1
Lund, K.P.2
Neil, D.A.3
-
23
-
-
4043127509
-
-
Laine, R. M.; Sellinger, A.; Chu, V.; Viney, C. J. Polym. Sci., A: Polym. Chem. 1994, 32, 3069-3089.
-
(1994)
J. Polym. Sci., A: Polym. Chem.
, vol.32
, pp. 3069-3089
-
-
Laine, R.M.1
Sellinger, A.2
Chu, V.3
Viney, C.4
-
24
-
-
18944383666
-
-
Lewis, L. N.; Sy, K. G.; Bryant, G. L., Jr.; Donahue, P. E. Organometallics 1991, 10, 3750-3759.
-
(1991)
Organometallics
, vol.10
, pp. 3750-3759
-
-
Lewis, L.N.1
Sy, K.G.2
Bryant Jr., G.L.3
Donahue, P.E.4
-
25
-
-
85033819504
-
-
note
-
2. All other chemicals were used as received.
-
-
-
-
26
-
-
0022028208
-
-
Laub, R. J.; Finkelmann, H.; Apfel, M. A.; Janini, G. M.; Lühmann, B. H.; Price, A.; Roberts, W. L.; Shaw, T. J.; Smith, C. A. Anal. Chem. 1985, 57, 651.
-
(1985)
Anal. Chem.
, vol.57
, pp. 651
-
-
Laub, R.J.1
Finkelmann, H.2
Apfel, M.A.3
Janini, G.M.4
Lühmann, B.H.5
Price, A.6
Roberts, W.L.7
Shaw, T.J.8
Smith, C.A.9
-
27
-
-
85033821066
-
-
note
-
n = 1010, PDI = 1.27. Mass spectral results (EI): m/z and intensities for tri-, tetra-, and pentasubstituted species within I are 797, 4.9%; 921, 3.8%; and 1045, 1.1%, respectively.
-
-
-
-
28
-
-
85033822943
-
-
note
-
n = 1860, PDI = 1.40.
-
-
-
-
29
-
-
85033825909
-
-
note
-
2 methylene being hydrosilylated to a methyl group. One likely product is the intramolecular hydrosilylation product: (Equation Presented)
-
-
-
-
30
-
-
3343015879
-
-
John Wiley and Sons: New York
-
Mark, H. F.; Bikales, N. M.; Overberger, C. G.; Menges, G., Eds. Encyclopedia of Polymer Science and Engineering, 2nd ed.; John Wiley and Sons: New York, 1989; Vol. 15, p 251.
-
(1989)
Encyclopedia of Polymer Science and Engineering, 2nd Ed.
, vol.15
, pp. 251
-
-
Mark, H.F.1
Bikales, N.M.2
Overberger, C.G.3
Menges, G.4
-
32
-
-
85033806147
-
-
Urban, M. W., Craver, C. D., Eds.; American Chemical Society: Washington, DC
-
Simonsick, W. J. In Structure-Property Relations in Polymers: Spectroscopy and Performance; Urban, M. W., Craver, C. D., Eds.; American Chemical Society: Washington, DC, 1993; No. 711.
-
(1993)
Structure-Property Relations in Polymers: Spectroscopy and Performance
, vol.711
-
-
Simonsick, W.J.1
-
33
-
-
85033821755
-
-
note
-
The product mixture, obtained on reacting 4 equiv of propargyl methacrylate with the octahydrido cubes, is very complex. Product distributions per reaction 1 ensure a set of α and β isomers. A statistical distribution of products without isomers should be ≈3% mono, ≈11% di, ≈22% tri, ≈27% tetra, ≈22% penta, ≈11% hexa, ≈3% hepta, and ≈0.4% octa. Additionally, the products contain vinylsiloxane moieties resembling the vinylsiloxane environment of Karstedt's catalyst [Pt(dvs)]. Thus, formation of one or two such moieties on the same edge of either cube might stabilize the active catalyst species and keep it on the cube face where it can react further, i.e., intra- and intermolecular hydrosilylation. Taken in toto, a nonstatistical product distribution is expected and found.
-
-
-
-
36
-
-
85033830996
-
-
unpublished work
-
Abrasion resistance studies will be reported at a later date. Sellinger, A.; Laine, R. M., unpublished work.
-
-
-
Sellinger, A.1
Laine, R.M.2
|