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66249134947
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25
-
-
70349925894
-
-
The oxidation potentials for the ferrocene moiety in 1 and 2 were 475 and 95 mV, respectively, against the ferrocene/ferrocenium redox pair. The aminobenzyl and aminobenzoate groups in 2 showed irreversible electrochemical oxidation at 475 and 620 mV, respectively
-
(b)The oxidation potentials for the ferrocene moiety in 1 and 2 were 475 and 95 mV, respectively, against the ferrocene/ferrocenium redox pair. The aminobenzyl and aminobenzoate groups in 2 showed irreversible electrochemical oxidation at 475 and 620 mV, respectively.
-
-
-
-
26
-
-
70349918532
-
-
See the Supporting Information
-
See the Supporting Information.
-
-
-
-
27
-
-
70349910352
-
-
Numberings for norbornenes are used here
-
Numberings for norbornenes are used here.
-
-
-
-
28
-
-
34250775929
-
-
Lin, N.-T.; Lin, S.-Y.; Lee, S.-L.; Chen, C.-h.; Hsu, C.-H.; Hwang, L.-P.; Xie, Z.-Y.; Chen, C.-H.; Huang, S.-L.; Luh, T.-Y. Angew. Chem., Int. Ed. 2007, 46, 4481-4485.
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0000509154
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0001974818
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For a review, see
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0016917550
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34
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0000711840
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Wai, J. S. M.; Marko, I.; Svendsen, J. S.; Finn, M. G.; Jacobsen, E. N.; Sharpless, K. B. J. Am. Chem. Soc. 1989, 111, 1123-1125.
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-
36
-
-
70349923815
-
-
The absorptions for the CHOH carbons in single-stranded poly(norbornandiol) (16) were found at δ 72.7.
-
The absorptions for the CHOH carbons in single-stranded poly(norbornandiol) (16) were found at δ 72.7.
-
-
-
-
37
-
-
4544323061
-
-
Diols are known to form hydrogen bonding with another diol in solid. For example
-
Diols are known to form hydrogen bonding with another diol in solid. For example: Salem, B.; Suffert, J. Angew. Chem., Int. Ed. 2004, 43, 2826-2830.
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Salem, B.1
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38
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54249113253
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Ito, H.; Furusho, Y.; Hasegawa, T.; Yashima, E. J. Am. Chem. Soc. 2008, 130, 14008-14015.
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Ito, H.1
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-
39
-
-
12344327390
-
-
Examples are known on the hydrogen bonding between a diol moiety and a carbonyl group of an ester in solid. For example
-
Examples are known on the hydrogen bonding between a diol moiety and a carbonyl group of an ester in solid. For example: Kelly, T. R.; Cai, X.; Tu, B.; Elliott, E. L.; Grossmann, G.; Laurent, P. Org. Lett. 2004, 6, 4953-4956.
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Kelly, T.R.1
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Elliott, E.L.4
Grossmann, G.5
Laurent, P.6
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40
-
-
0000252132
-
-
McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388-3390.
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Condon, B.D.4
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41
-
-
70349925900
-
-
Calculation based on a 12-mer with two styrene and two vinyl end groups
-
(a) Calculation based on a 12-mer with two styrene and two vinyl end groups.
-
-
-
-
42
-
-
70349910344
-
-
Calculation based on the product with complete dihydroxylation of all double bonds in a 12-mer 6 with two styrene and two vinyl end groups plus 24 water molecules because polymer 15 may be hygroscopic
-
(b) Calculation based on the product with complete dihydroxylation of all double bonds in a 12-mer 6 with two styrene and two vinyl end groups plus 24 water molecules because polymer 15 may be hygroscopic.
-
-
-
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