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3
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0033517692
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Green M.M., Park J.-W., Sato T., Teramoto A., Lifson S., Selinger R.L.B., and Selinger J.V. Angew. Chem., Int. Ed. 38 (1999) 3138
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Green, M.M.1
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Selinger, J.V.7
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11
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0031117834
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For example, see:
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For example, see:. Pu L. Acta Polym. 48 (1997) 116
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Acta Polym.
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Pu, L.1
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12
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0000718373
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Pu L. Chem. Rev. 98 (1997) 2405
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(1997)
Chem. Rev.
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Pu, L.1
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13
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33846368901
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Diederich F., Stang P.J., and Tykwinski R.R. (Eds), Wiley-VCH, Weinheim, Germany
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Pu L. In: Diederich F., Stang P.J., and Tykwinski R.R. (Eds). Acetylene Chemistry: Chemistry, Biology, and Material Science (2004), Wiley-VCH, Weinheim, Germany 453-494
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Acetylene Chemistry: Chemistry, Biology, and Material Science
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Pu, L.1
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18
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14844320755
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Onouchi H., Miyagawa T., Furuko A., Maeda K., and Yashima E. J. Am. Chem. Soc. 127 (2005) 2960
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Onouchi, H.1
Miyagawa, T.2
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Maeda, K.4
Yashima, E.5
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19
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0035542909
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Hill D.J., Mio M.J., Prince R.B., Hughes T.S., and Moore J.S. Chem. Rev. 101 (2001) 3893
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Chem. Rev.
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Hill, D.J.1
Mio, M.J.2
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Moore, J.S.5
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22
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24344436799
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Morisaki Y., Ouchi Y., Fukui T., Naka K., and Chujo Y. Tetrahedron Lett. 46 (2005) 7011
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Morisaki, Y.1
Ouchi, Y.2
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Naka, K.4
Chujo, Y.5
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23
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0031647058
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-
Few polymers comprising a chiral heteroatom have been reported to date; for Si atom:
-
Few polymers comprising a chiral heteroatom have been reported to date; for Si atom:. Kawakami Y., Takeyama K., Komuro K., and Ooi O. Macromolecules 31 (1998) 551
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(1998)
Macromolecules
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Kawakami, Y.1
Takeyama, K.2
Komuro, K.3
Ooi, O.4
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25
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0342763378
-
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For S atom:
-
For S atom:. Angeloni A., Laus M., Caretti D., Chiellini E., and Galli G. Makromol. Chem. 191 (1990) 2787
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(1990)
Makromol. Chem.
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Angeloni, A.1
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Caretti, D.3
Chiellini, E.4
Galli, G.5
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27
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1642496767
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Sokolov and co-workers analyzed a transition from dynamics characteristics for small molecules to the Rouse dynamics characteristic for polymers in poly(dimethylsiloxane) (PDMS):
-
Sokolov and co-workers analyzed a transition from dynamics characteristics for small molecules to the Rouse dynamics characteristic for polymers in poly(dimethylsiloxane) (PDMS):. Ding Y., Kisliuk A., and Sokolov A.P. Macromolecules 37 (2004) 161
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Macromolecules
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Ding, Y.1
Kisliuk, A.2
Sokolov, A.P.3
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28
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0032564850
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Imamoto T., Watanabe J., Wada Y., Masuda H., Yamada H., Tsuruta H., Matsukawa S., and Yamaguchi K. J. Am. Chem. Soc. 120 (1998) 1635
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Imamoto, T.1
Watanabe, J.2
Wada, Y.3
Masuda, H.4
Yamada, H.5
Tsuruta, H.6
Matsukawa, S.7
Yamaguchi, K.8
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29
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0037117635
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Wild and co-workers reported the synthesis and isolation of three kinds of optically active hexaphosphines having four chiral phosphorus atoms by another approach, and a unique double-stranded parallel helicate of the copper complex was characterized:
-
Wild and co-workers reported the synthesis and isolation of three kinds of optically active hexaphosphines having four chiral phosphorus atoms by another approach, and a unique double-stranded parallel helicate of the copper complex was characterized:. Bowyer P.K., Vernon C.C., Nahid G.-N., Gugger P.A., Rae A.D., Swiegers G.F., Willis A.C., Zank J., and Wild S.B. Proc. Natl. Acad. Sci. USA 99 (2002) 4877
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Bowyer, P.K.1
Vernon, C.C.2
Nahid, G.-N.3
Gugger, P.A.4
Rae, A.D.5
Swiegers, G.F.6
Willis, A.C.7
Zank, J.8
Wild, S.B.9
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30
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33846348432
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-
note
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+: 781.6574, found 781.6560.
-
-
-
-
31
-
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33846364729
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-
note
-
Octaphosphine (S,R,S,R,R,S,R,S)-4 exhibited decomposition at approximately 220 °C before melting due to the dissociation of boranes according to the thermogravimetric analysis (TGA).
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-
-
-
32
-
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33846344428
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-
note
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This sample was pre-heated up to 110 °C in the first cycle.
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-
-
-
33
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0034031562
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For examples, see:
-
For examples, see:. Shirota Y. J. Mater. Chem. 10 (2000) 1
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(2000)
J. Mater. Chem.
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, pp. 1
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Shirota, Y.1
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35
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19444372309
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Imae and Kawakami reported molecular glasses based on silicon-containing well-defined oligomers:
-
Imae and Kawakami reported molecular glasses based on silicon-containing well-defined oligomers:. Imae I., and Kawakami Y. Chem. Lett. 34 (2005) 290
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Chem. Lett.
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Imae, I.1
Kawakami, Y.2
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36
-
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33846402222
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-
note
-
Optically inactive bisphosphine 1′ was prepared according to the Imamoto's procedure without (-)-sparteine. See also Ref. 7.
-
-
-
-
37
-
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33846374870
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note
-
This point would be worth considering. The effort to clarify the crystallinity of other optically pure enantiomers is currently underway.
-
-
-
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38
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33846379696
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-
note
-
Optically inactive tetraphosphine 2′ and hexaphosphine 3′ exhibited the broad diffraction peaks and the halo peak, respectively.
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