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2955, 1592, 1505, 1451, 1372, 1320, 1288, 1255, 1228, 1105, 1066,
1006, 811, 739, 670, 577, 527. 1H NMR (400 MHz, DMSO)
8.58 (s,
d
2H), 7.83 (d, J ¼ 8.3 Hz, 4H), 7.77e7.79 (m, 2H), 7.73 (d, J ¼ 8.3 Hz,
4H), 7.65e7.68 (m, 2H), 7.30e7.35 (m, 4H), 0.68 (s, 6H). 13C NMR
(100 MHz, DMSO):
d 144.4, 143.7, 137.6, 137.4, 136.1, 133.4, 124.0,
123.5, 123.0, 120.5, 111.2, ꢁ2.3. HRMS (FAB) calcd for C28H24N4Si
(MHþ): 445.1843, found 445.1829. Anal. Calcd for C28H24N4Si: C,
75.64; H, 5.44; N, 12.60. Found: C, 75.60; H, 5.35; N, 12.69.
Bis(4-(benimidazol-1-yl)phenyl)diphenylsilane (3b) was affor-
ded as a gray solid. Yield: 45.1%. IR (KBr pellet cmꢁ1): 3056, 1594,
1501, 1453, 1376, 1290, 1232, 1194, 1109, 1011, 974, 829, 741, 701, 641,
582, 535. 1H NMR (400 MHz, DMSO)
d 8.58 (s, 2H), 7.83 (d,
J ¼ 8.3 Hz, 4H), 7.77e7.80 (m, 6H), 7.72e7.74 (m, 2H), 7.60e7.63 (m,
4H), 7.50e7.55 (m, 6H), 7.32e7.35 (m, 4H). 13C NMR (100 MHz,
DMSO):
d 143.9, 143.1, 137.5, 137.4, 135.8, 134.4, 132.7, 132.6, 130.1,
128.3, 127.8, 123.5, 123.1, 122.5, 119.9, 110.1. HRMS (FAB) calcd for
C38H28N4Si (MHþ): 569.2075, found 569.2082. Anal. Calcd for
C38H28N4Si: C, 80.25; H, 4.96; N, 9.85. Found: C, 80.20; H, 4.93; N,
9.89.
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Bis(3-(benzimidazol-1-yl)phenyl)dimethylsilane
(3c)
was
afforded as a light yellow solid. Yield: 50.7%. IR (KBr pellet cmꢁ1):
3055, 3032, 2955, 1591, 1493, 1451, 1399, 1289, 1254, 1228, 1199,
1108, 1043, 1002, 827, 787, 741, 694, 617, 538. 1H NMR (400 MHz,
DMSO, ppm)
7.58e7.72 (m, 6H), 7.50 (d, J ¼ 5.5 Hz, 2H), 7.23e7.31 (m, 4H), 0.70 (s,
6H). 13C NMR (100 MHz, DMSO, ppm):
144.6, 142.8, 141.9, 138.2,
d
8.58 (s, 2H), 7.83 (s, 2H), 7.77 (d, J ¼ 8.3 Hz, 2H),
d
137.1, 136.1, 132.9, 130.3, 129.9, 126.0, 122.1, 118.7, 111.3, ꢁ2.6. HRMS
(FAB) calcd for C28H24N4Si (MHþ): 445.1843, found 445.1856. Anal.
Calcd for C28H24N4Si: C, 75.64; H, 5.44; N, 12.60. Found: C, 75.61; H,
5.42; N, 12.65.
Acknowledgments
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This research was supported by the National Natural Science
Foundation of China (No. 21274080), Postdoctoral Science Foun-
dation of China (No. 2012M511018), the Key Natural Science
Foundation of Shandong Province of China (No. ZR2011BZ001) and
Special Funds for Postdoctoral Innovative Projects of Shandong
Province (No. 201103037).
Appendix A. Supplementary data
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12 (2010) 1041e1043.
Supplementary data related to this article can be found at http://
[47] D.X. Wang, Synthesis, Assembly and Properties of N-heterocycle and
Carboxylate Functionalized Silanes, Shandong University Doctoral Disserta-
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