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Volumn 36, Issue 8, 1997, Pages 836-838

Carbon Networks Based on Dehydrobenzoannulenes: Synthesis of Graphdiyne Substructures

Author keywords

Alkynes; Annulenes; Aromaticity; Carbon allotropes

Indexed keywords


EID: 0031007781     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199708361     Document Type: Article
Times cited : (459)

References (38)
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    • (1992) Angew. Chem. , vol.104 , pp. 1123-1146
    • Diederich, F.1    Rubin, Y.2
  • 2
    • 33748231383 scopus 로고
    • a) F. Diederich, Y. Rubin, Angew. Chem. 1992, 104, 1123-1146; Angew. Chem. Int. Ed. Engl. 1992, 31, 1101-1123;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 1101-1123
  • 4
    • 0003799267 scopus 로고
    • (Eds.: P. J. Stang, F. Diederich), VCH, Weinheim
    • c) F. Diederich in Modern Acetylene Chemistry (Eds.: P. J. Stang, F. Diederich), VCH, Weinheim, 1995;
    • (1995) Modern Acetylene Chemistry
    • Diederich, F.1
  • 5
    • 0000864109 scopus 로고
    • d) U. H. F. Bunz, Angew. Chem. 1994, 106, 1127-1132; Angew. Chem. Int. Ed. Engl. 1994, 33, 1073-1076;
    • (1994) Angew. Chem. , vol.106 , pp. 1127-1132
    • Bunz, U.H.F.1
  • 6
    • 33748224004 scopus 로고
    • d) U. H. F. Bunz, Angew. Chem. 1994, 106, 1127-1132; Angew. Chem. Int. Ed. Engl. 1994, 33, 1073-1076;
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1073-1076
  • 10
    • 33748823242 scopus 로고
    • Y. Rubin, C. B. Knobler, F. Diederich, Angew. Chem. 1991, 103, 708-710; Angew. Chem. Int. Ed. Engl. 1991, 30, 698-700.
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 698-700
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    • 33748243060 scopus 로고
    • J.-D. van Loon, P. Seiler, F. Diederich, Angew. Chem. 1993, 105, 1235-1237; Angew. Chem. Int. Ed. Engl. 1993, 32, 1187-1189.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 1187-1189
  • 14
    • 33748225267 scopus 로고
    • T. Lange, V. Gramlich, W. Amrein, F. Diederich, M. Gross, C. Boudon, J.-P. Gisselbrecht, Angew. Chem. 1995, 107, 898-901; Angew. Chem. Int. Ed. Engl. 1995, 34, 805-809.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 805-809
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    • 33748216485 scopus 로고
    • J. Anthony, C. B. Knobler, F. Diederich, Angew. Chem. 1993, 105, 437-440; Angew. Chem. Int. Ed. Engl. 1993, 32, 406-409.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 406-409
  • 17
    • 0642288394 scopus 로고    scopus 로고
    • private communication. This value can also be calculated from the numbers in Table 5 of ref. [2]
    • R. Baughman, private communication. This value can also be calculated from the numbers in Table 5 of ref. [2].
    • Baughman, R.1
  • 18
    • 0642349681 scopus 로고    scopus 로고
    • note
    • The term graphdiyne comes from the name graphyne [2], which in turn is derived from graphite. Graphyne, the monoacetylenic analogue of 1, can be viewed as resulting from replacement of one-third of the carbon-carbon bonds in graphite by -C≡C-linkages. It follows that the diacetylenic version be called graphdiyne.
  • 30
  • 34
    • 0642349680 scopus 로고    scopus 로고
    • 2
    • 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.