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0000071951
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ed. by Z. Rappoport, Y. Apeloig, John Wiley & Sons, New York, Chap. 3
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Grützmacher, H.1
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7
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37049084284
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For theoretical studies on germabicyclobutanes, see
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Nagase, S.1
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Lee, V.Y.1
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2942703958
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For compounds with an inverted-tetrahedral configuration, see
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For compounds with an inverted-tetrahedral configuration, see: A. F. Richards, M. Brynda, M. M. Olmstead, P. P. Power, Organometallics 2004, 23, 2841;
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Richards, A.F.1
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4344600550
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A. F. Richards, M. Brynda, P. P. Power, Organometallics 2004, 23, 4009.
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Richards, A.F.1
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37049075359
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D. Bravo-Zhivotovskii, I. Zharov, M. Kapon, Y. Apeloig, J. Chem. Soc., Chem. Commun. 1995, 1625.
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Bravo-Zhivotovskii, D.1
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14
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45449113052
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2: yellow-orange crystals; mp 203.7-205.5°C; 1H NMR (C6D6, δ) 0.44 (s, 12H, SiCH3, 1.30 (s, 18H, t-Bu, 1.72-2.46 (m, 28H, adamantylidene, 13C NMR (C6D6, δ, 0.2 (CH3, 20.3 (C(CH3)3, 28.1 (C(CH3) 3, 29.5, 39.8, 42.5, 43.5, 44.7, 45.4, 135.4 (ring carbon, 29Si NMR (C6D6, δ) 11.1; UV-vis (n-hexane) λmax/nm (ε/103) 325 (4.0) 440 (9.8, MS (EI, 70eV) m/z, ) 646 (76, M, 589 (51, 531 (16, 474 (6, 73 100, HRMS m/z calcd for C32H 58Ge2Si2, 646.2501; found, 646.2503. For experimental details including synthesis of 3, see Supporting Information
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2, 646.2501; found, 646.2503. For experimental details including synthesis of 3, see Supporting Information.
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15
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45449102949
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Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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16
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45449087157
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6) have been deposited with Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 680574.
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6) have been deposited with Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 680574.
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17
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0001587955
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T. Tsumuraya, S. Sato, W. Ando, Organometallics 1990, 9, 2061.
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Tsumuraya, T.1
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18
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0000849169
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L. Párkányi, A. Kaiman, S. Sharma, D. M. Nolen, K. H. Pannel, Inorg. Chem. 1994, 33, 180.
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Párkányi, L.1
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Nolen, D.M.4
Pannel, K.H.5
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19
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45449083512
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Details for the DFT calculations, see Supporting Information
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Details for the DFT calculations, see Supporting Information.
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20
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45449091639
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The greater relative stability of LB isomer to SB isomer of parent bicyclo[1.1.0]tetragermane than parent bicyclotetrasilane has been predicted theoretically by Nagase et al.
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The greater relative stability of LB isomer to SB isomer of parent bicyclo[1.1.0]tetragermane than parent bicyclotetrasilane has been predicted theoretically by Nagase et al.
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21
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45449119544
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16 and digermirane 4 (300 nm (ε 17400)).
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16 and digermirane 4 (300 nm (ε 17400)).
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23
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0009335148
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H. K. Sharma, F. Cervantes-Lee, L. Párkányi, K. H. Pannel, Organometallics 1996, 15, 429.
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Sharma, H.K.1
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Párkányi, L.3
Pannel, K.H.4
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45449103156
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max = 409 nm, f = 0.188 and LB-6′.
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max = 409 nm, f = 0.188 and LB-6′.
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25
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45449098149
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13CNMR chemical shift between SB and LB isomers provides a good index to distinguish the isomers.
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13CNMR chemical shift between SB and LB isomers provides a good index to distinguish the isomers.
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