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0001029702
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See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
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17
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33751386331
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See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
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Tanaka, K.5
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18
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20544447483
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See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
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Toyohara, K.1
Nagao, H.2
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Yoshida, T.4
Tanaka, K.5
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19
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0029252180
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See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
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Hankka, M.1
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Pakkanen, T.A.4
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20
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0029854428
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(a) Gibson, D. H.; Ding, Y.; Sleadd, B. A.; Franco, J. O.; Richardson, J. F.; Mashuta, M. S. J. Am. Chem. Soc. 1996, 118, 11984.
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21
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0000702957
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(b) Gibson, D. H.; Sleadd, B. A.; Mashuta, M. S.; Richardson, J. F. Organometallics 1997, 16, 4421.
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Richardson, J.F.4
-
23
-
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11644309057
-
-
note
-
3OD): δ 203.98, 194.44, 156.59, 153.74, 139.24, 127.80, 124.68, 70.05.
-
-
-
-
24
-
-
11644254740
-
-
note
-
3CN): δ 203.06, 194.37, 171.70, 156.29, 153.89, 139.52, 127.96, 124.40, 69.33, 20.98.
-
-
-
-
25
-
-
85087242539
-
-
note
-
1/n; a = 9.7402(2) A, b = 15.8826(4) A°, c = 11.2409(2) A°, α= 90°, β= 107.905(1)°, γ= 90°. Final R indices (I > 2σ(I)): R1 = 0.0390, wR2 = 0.0768.
-
-
-
-
26
-
-
11644291314
-
-
note
-
Additional commentary about the structure and ORTEP packing diagrams are available in the Supporting Information.
-
-
-
-
27
-
-
11644258587
-
-
note
-
3OD): δ 199.97, 194.26, 157.50, 154.07, 141.24, 128.60, 125.07, 61.60.
-
-
-
-
28
-
-
11644274804
-
-
note
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12
-
-
-
-
29
-
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0004150157
-
-
Program Library for Structure Solution and Molecular Graphics; Siemens Analytical Instruments Division: Madison, WI
-
SHELXTL 5.03 (PC-version), Program Library for Structure Solution and Molecular Graphics; Siemens Analytical Instruments Division: Madison, WI, 1995.
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(1995)
SHELXTL 5.03 (PC-version)
-
-
-
30
-
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33947338539
-
-
note
-
4, the formaldehyde hemiacetal is present in low yield (diminished by partial removal with solvent).
-
-
-
-
31
-
-
0004284856
-
-
McGraw Hill: Maidenhead, England
-
Addition of dimedone to the mixture results in slow disappearance of the resonance at δ 4.64 and formation of the dimedoneformaldehyde derivative (compared with an authentic sample: Kemp, W. Qualitative Organic Analysis; McGraw Hill: Maidenhead, England, 1986; p 89).
-
(1986)
Qualitative Organic Analysis
, pp. 89
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Kemp, W.1
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34
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0001613088
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Lucia, L. A.; Burton, R. D.; Schanze, K. S. Inorg. Chim. Acta 1993, 208, 103.
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Inorg. Chim. Acta
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Lucia, L.A.1
Burton, R.D.2
Schanze, K.S.3
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35
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0000638813
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Stufkens, D.J.4
Vlcek Jr., A.5
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0000866021
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Nietlispach, D.; Yeghini, D.; Berke, H. Helv. Chim. Acta 1994, 77, 2197.
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39
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0000737069
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Ayllón, J. A.; Gervaux, C.; Sabo-Etienne, S.; Chaudret, B. Organometallics 1997, 16, 2000.
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Chaudret, B.4
-
40
-
-
11644284980
-
-
note
-
4; after filtration, the filtrate was concentrated to 20 mL. Hexane was then added to effect precipitation of 0.34 g (83% yield) of 5.
-
-
-
-
42
-
-
11644264038
-
-
note
-
1H NMR showed an acetoxy methyl resonance at δ 1.91 and resonances for bipyridyl protons which are distinct from 6; the ratio of the two compounds was 2:1 of the unknown to 6). Continued photolysis, or evaporation of solvent and redissolution, resulted in conversion of the second compound to 6. Samples were too dilute to provide meaningful IR spectral data.
-
-
-
-
43
-
-
11644264471
-
-
note
-
2 had identical spectral properties.
-
-
-
-
44
-
-
0001704975
-
-
Gogoll, A.; Örnebro, J.; Grennberg, H.; Bäckvall, J.-E. J. Am. Chem. Soc. 1994, 116, 6, 3631.
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47
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0010884104
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(c) Lin, Y. C.; Milstein, D.; Wreford, S. S. Organometallics 1983, 2, 1461.
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Lin, Y.C.1
Milstein, D.2
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