SCOPUS 정보 검색 플랫폼

Volumn 46, Issue 42, 2010, Pages 8008-8010

Fabrication and transformation of novel two-dimensional tripod structures: Structural modulation by alkyl chain length and tandem Claisen rearrangement

(4) Omori, Kazuhiro a,b,c Kikkawa, Yoshihiro b Kanesato, Masatoshi b Hiratani, Kazuhisa c

a Industrial Technology Center of Tochigi prefecture (Japan)

b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST (Japan)

c UTSUNOMIYA UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL GROUP; ETHER DERIVATIVE; ISOBUTYLENE; NANOMATERIAL;

ARTICLE; BIOTRANSFORMATION; CHEMICAL STRUCTURE; CLAISEN REARRANGEMENT; NANOFABRICATION; SCANNING ELECTRON MICROSCOPY; SCANNING TUNNELLING MICROSCOPY; TANDEM CLAISEN REARRANGEMENT;

EID: 77958462949 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/c0cc02963g Document Type: Article

Times cited : (17)

References (25)

1
- 29644441516
- M. W. Hosseini Chem. Commun. 2005 5825
- (2005) Chem. Commun. , pp. 5825
- Hosseini, M.W.¹

2
- 68749104860
- J. D. West Chem. Commun. 2005 5830
- (2005) Chem. Commun. , pp. 5830
- West, J.D.¹

3
- 20344402526
- M. W. Hosseini Acc. Chem. Res. 2005 38 313
- (2005) Acc. Chem. Res. , vol.38 , pp. 313
- Hosseini, M.W.¹

4
- 33749521115
- P. Dechambenoit S. Ferlay M. W. Hosseini J.-M. Planeix N. Kyritsakas New J. Chem. 2006 30 1403
- (2006) New J. Chem. , vol.30 , pp. 1403
- Dechambenoit, P.¹ Ferlay, S.² Hosseini, M.W.³ Planeix, J.-M.⁴ Kyritsakas, N.⁵

5
- 61849132151
- A. Ciesielski G. Schaeffer A. Petitjean J.-M. Lehn P. Samorì Angew. Chem., Int. Ed. 2009 48 2039
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 2039
- Ciesielski, A.¹ Schaeffer, G.² Petitjean, A.³ Lehn, J.-M.⁴ Samorì, P.⁵

6
- 4344582312
- M. Ruben J. Rojo F. J. Romero-Salguero L. H. Uppadine J.-M. Lehn Angew. Chem., Int. Ed. 2004 43 3644
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 3644
- Ruben, M.¹ Rojo, J.² Romero-Salguero, F.J.³ Uppadine, L.H.⁴ Lehn, J.-M.⁵

7
- 2342444706
- M. A. Lingenfelder H. Spillmann A. Dmitriev S. Stepanow N. Lin J. V. Barth K. Kern Chem.-Eur. J. 2004 10 1913
- (2004) Chem.-Eur. J. , vol.10 , pp. 1913
- Lingenfelder, M.A.¹ Spillmann, H.² Dmitriev, A.³ Stepanow, S.⁴ Lin, N.⁵ Barth, J.V.⁶ Kern, K.⁷

8
- 33645510279
- J. Pansanel A. Jouaiti S. Ferlay M. W. Hosseini J.-M. Planeix N. Kyritsakas New J. Chem. 2006 30 71
- (2006) New J. Chem. , vol.30 , pp. 71
- Pansanel, J.¹ Jouaiti, A.² Ferlay, S.³ Hosseini, M.W.⁴ Planeix, J.-M.⁵ Kyritsakas, N.⁶

9
- 33846097220
- M. Surin P. Samorì A. Jouaiti N. Kyritsakas M. W. Hosseini Angew. Chem., Int. Ed. 2006 46 245
- (2006) Angew. Chem., Int. Ed. , vol.46 , pp. 245
- Surin, M.¹ Samorì, P.² Jouaiti, A.³ Kyritsakas, N.⁴ Hosseini, M.W.⁵

10
- 65549132379
- A. Ciesielski L. Piot P. Samorì A. Jouaiti M. W. Hosseini Adv. Mater. 2009 21 1131
- (2009) Adv. Mater. , vol.21 , pp. 1131
- Ciesielski, A.¹ Piot, L.² Samorì, P.³ Jouaiti, A.⁴ Hosseini, M.W.⁵

11
- 25144510978
- F. Tao S. L. Bernasek J. Am. Chem. Soc. 2005 127 12750
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 12750
- Tao, F.¹ Bernasek, S.L.²

12
- 33749515457
- J. Puigmart-Luis A. Minoia H. Uji-I C. Rovira J. Cornil S. De Feyter R. Lazzaroni D. B. Amabilino J. Am. Chem. Soc. 2006 128 12602
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 12602
- Puigmart-Luis, J.¹ Minoia, A.² Uji-I, H.³ Rovira, C.⁴ Cornil, J.⁵ De Feyter, S.⁶ Lazzaroni, R.⁷ Amabilino, D.B.⁸

13
- 33645472659
- K. G. Nath O. Ivasenko J. A. Miwa H. Dang J. D. Wuest A. Nanci D. F. Perepichka F. Rosei J. Am. Chem. Soc. 2006 128 4212
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 4212
- Nath, K.G.¹ Ivasenko, O.² Miwa, J.A.³ Dang, H.⁴ Wuest, J.D.⁵ Nanci, A.⁶ Perepichka, D.F.⁷ Rosei, F.⁸

14
- 34547838189
- M. Stöhr M. Wahl H. Spillmann L. H. Gade T. A. Jung Small 2007 3 1336
- (2007) Small , vol.3 , pp. 1336
- Stöhr, M.¹ Wahl, M.² Spillmann, H.³ Gade, L.H.⁴ Jung, T.A.⁵

15
- 70349921522
- M. Lackinger W. M. Heckl Langmuir 2009 25 11307
- (2009) Langmuir , vol.25 , pp. 11307
- Lackinger, M.¹ Heckl, W.M.²

16
- 75149128561
- T. Chen D. Wang X. Zhang Q.-L. Zhou R.-B. Zhang L.-J. Wan J. Phys. Chem. C 2010 114 533
- (2010) J. Phys. Chem. C , vol.114 , pp. 533
- Chen, T.¹ Wang, D.² Zhang, X.³ Zhou, Q.-L.⁴ Zhang, R.-B.⁵ Wan, L.-J.⁶

17
- 77952335976
- A. R. Ramesh K. G. Thomas Chem. Commun. 2010 46 3457
- (2010) Chem. Commun. , vol.46 , pp. 3457
- Ramesh, A.R.¹ Thomas, K.G.²

18
- 33845917799
- K. Tahara S. Furukawa H. Uji-I T. Uchino T. Ichikawa J. Zhang W. Mandouh M. Sonoda F. C. De Schryver S. De. Feyter Y. Tobe J. Am. Chem. Soc. 2006 128 16613
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 16613
- Tahara, K.¹ Furukawa, S.² Uji-I, H.³ Uchino, T.⁴ Ichikawa, T.⁵ Zhang, J.⁶ Mandouh, W.⁷ Sonoda, M.⁸ De Schryver, F.C.⁹ De. Feyter, S.¹⁰ Tobe, Y.¹¹

19
- 33645468527
- M. Lackinger S. Griessl L. Kampschulte F. Jamitzky W. M. Heckl Small 2005 1 532
- (2005) Small , vol.1 , pp. 532
- Lackinger, M.¹ Griessl, S.² Kampschulte, L.³ Jamitzky, F.⁴ Heckl, W.M.⁵

20
- 54449097179
- K. Hiratani M. Albrecht Chem. Soc. Rev. 2008 37 2413
- (2008) Chem. Soc. Rev. , vol.37 , pp. 2413
- Hiratani, K.¹ Albrecht, M.²

21
- 76749108016
- J. Hao K. Hiratani N. Kameta T. Oba J. Inclusion Phenom. Macrocyclic Chem. 2009 65 257
- (2009) J. Inclusion Phenom. Macrocyclic Chem. , vol.65 , pp. 257
- Hao, J.¹ Hiratani, K.² Kameta, N.³ Oba, T.⁴

22
- 75749136173
- K. Omori Y. Kikkawa H. Tokuhisa M. Kanesato K. Hiratani Colloids Surf., A 2010 356 58
- (2010) Colloids Surf., A , vol.356 , pp. 58
- Omori, K.¹ Kikkawa, Y.² Tokuhisa, H.³ Kanesato, M.⁴ Hiratani, K.⁵

23
- 1242329153
- A. D. Bond New J. Chem. 2004 28 104
- (2004) New J. Chem. , vol.28 , pp. 104
- Bond, A.D.¹

24
- 33947500663
- Y. Kikkawa E. Koyama S. Tsuzuki K. Fujiwara K. Miyake H. Tokuhisa M. Kanesato Chem. Commun. 2007 1343
- (2007) Chem. Commun. , pp. 1343
- Kikkawa, Y.¹ Koyama, E.² Tsuzuki, S.³ Fujiwara, K.⁴ Miyake, K.⁵ Tokuhisa, H.⁶ Kanesato, M.⁷

25
- 34249869272
- The alkyl chains in the building blocks of Cn-1 (n = odd) is slid along the long axis due to the oxygen atoms connected to the naphthalene unit. Therefore, the terminal methyl groups of the components in the building blocks have little steric repulsion
- F. Tao S. L. Bernasek Chem. Rev. 2007 107 1408
- (2007) Chem. Rev. , vol.107 , pp. 1408
- Tao, F.¹ Bernasek, S.L.²

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