SCOPUS 정보 검색 플랫폼

Organic and Biomolecular Chemistry

Volumn 4, Issue 20, 2006, Pages 3729-3745

Amplification of chirality in liquid crystals

(2) Eelkema, Rienk a Feringa, Ben L a

a UNIVERSITY OF GRONINGEN (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHIRALITY; DOPANT SYSTEMS; SOLVENT-SOLUTE INTERACTION; SUPRAMOLECULAR ASSEMBLIES;

CRYSTALLINE MATERIALS; DOPING (ADDITIVES); INTELLIGENT MATERIALS; LIQUID CRYSTAL DISPLAYS; SOLVENTS; SUPRAMOLECULAR CHEMISTRY;

CHOLESTERIC LIQUID CRYSTALS;

EID: 33749579465 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b608749c Document Type: Article

Times cited : (292)

References (110)

1
- 0003594981
- Taylor and Francis, London
- P. J. Collins, M. Hird, Introduction to Liquid Crystals - Chemistry and Physics, Taylor and Francis, London, 1997
- (1997) Introduction to Liquid Crystals - Chemistry and Physics
- Collins, P.J.¹ Hird, M.²

2
- 0346920975
- Wiley-VCH, Weinheim
- I. Dierking, Textures of Liquid Crystals, Wiley-VCH, Weinheim, 2003
- (2003) Textures of Liquid Crystals
- Dierking, I.¹

3
- 0004130004
- P. J. Collins and J. S. Patel, Oxford University Press, New York, Oxford
- Handbook of Liquid Crystal Research, ed., P. J. Collins, and, J. S. Patel, Oxford University Press, New York, Oxford, 1997
- (1997) Handbook of Liquid Crystal Research, Ed.

4
- 0003872521
- D. Demus, J. Goodby, G. W. Gray, H.-W. Spiess and V. Vill, Wiley-VCH, Weinheim
- Handbook of Liquid Crystals, ed., D. Demus, J. Goodby, G. W. Gray, H.-W. Spiess, and, V. Vill, Wiley-VCH, Weinheim, 1998
- (1998) Handbook of Liquid Crystals, Ed.

5
- 0004091130
- H.-S. Kitzerow and C. Bahr, Springer-Verlag, New York
- Chirality in Liquid Crystals, ed., H.-S. Kitzerow, and, C. Bahr, Springer-Verlag, New York, 2001
- (2001) Chirality in Liquid Crystals, Ed.

6
- 34250554698
- F. Reinitzer Monatsh. Chem. 1888 9 421
- (1888) Monatsh. Chem. , vol.9 , pp. 421
- Reinitzer, F.¹

7
- 0000078816
- O. Lehmann Z. Phys. Chem. 1889 4 462
- (1889) Z. Phys. Chem. , vol.4 , pp. 462
- Lehmann, O.¹

8
- 0003634592
- Gordon & Breach, Philadelphia
- Chiral doped Smectic C liquid crystalline phases have shown interesting properties for potential future applications in ferroelectric devices in displays and telecommunication. However, they are beyond the scope of this Perspective. For general reviews of these phases, see ref. 2 and J. W. Goodby, R. Blinc, N. A. Clark, S. T. Lagerwall, M. A. Osipov, S. A. Pikin, T. Sakurai, K. Yoshino and B. Zeks, Ferroelectric Liquid Crystals: Principles, Properties and Applications, Gordon & Breach, Philadelphia, 1991
- (1991) Ferroelectric Liquid Crystals: Principles, Properties and Applications
- Goodby, J.W.¹ Blinc, R.² Clark, N.A.³ Lagerwall, S.T.⁴ Osipov, M.A.⁵ Pikin, S.A.⁶ Sakurai, T.⁷ Yoshino, K.⁸ Zeks, B.⁹

9
- 0035800389
- For reviews on chiral low molecular weight dopants:
- N. Tamaoki Adv. Mater. 2001 13 1135
- (2001) Adv. Mater. , vol.13 , pp. 1135
- Tamaoki, N.¹

10
- 2242424960
- G. Solladié R. G. Zimmermann Angew. Chem., Int. Ed. Engl. 1984 23 348
- (1984) Angew. Chem., Int. Ed. Engl. , vol.23 , pp. 348
- Solladié, G.¹ Zimmermann, R.G.²

11
- 0032439567
- G. P. Spada G. Proni Enantiomer 1998 3 301
- (1998) Enantiomer , vol.3 , pp. 301
- Spada, G.P.¹ Proni, G.²

12
- 0034795296
- For reviews on switching in liquid crystalline environments, see:
- G. Proni G. P. Spada Enantiomer 2001 6 171
- (2001) Enantiomer , vol.6 , pp. 171
- Proni, G.¹ Spada, G.P.²

13
- 0345850194
- K. Ichimura Chem. Rev. 2000 100 1847
- (2000) Chem. Rev. , vol.100 , pp. 1847
- Ichimura, K.¹

14
- 33644910136
- B. L. Feringa, Wiley-VCH, Weinheim, pp. 363-397
- T. Ikeda and A. Kanazawa, in Molecular Switches, ed., B. L. Feringa, Wiley-VCH, Weinheim, 2001 pp. 363-397
- (2001) Molecular Switches, Ed.
- Ikeda, T.¹ Kanazawa In, A.²

15
- 0043264187
- T. Ikeda J. Mater. Chem. 2003 13 2037
- (2003) J. Mater. Chem. , vol.13 , pp. 2037
- Ikeda, T.¹

16
- 33749565470
- 845
- In this Perspective, mesogenic groups are defined as functional groups that resemble the main structure of the mesogenic host, which is in accordance with IUPAC nomenclature. See: M. Baron, Pure Appl. Chem., 2001, 73, 845
- (2001) Pure Appl. Chem.
- Baron, M.¹

17
- 0001020996
- H. Finkelmann H. Stegemeyer Ber. Bunsen-Ges. Phys. Chem. 1978 82 1302
- (1978) Ber. Bunsen-Ges. Phys. Chem. , vol.82 , pp. 1302
- Finkelmann, H.¹ Stegemeyer, H.²

18
- 0035530343
- G. P. Semenkova L. A. Kutulya N. I. Shkol'nikova T. V. Khandrimailova Cryst. Rep. 2001 46 118
- (2001) Cryst. Rep. , vol.46 , pp. 118
- Semenkova, G.P.¹ Kutulya, L.A.² Shkol'Nikova, N.I.³ Khandrimailova, T.V.⁴

19
- 0001732704
- H.-G. Kuball H. Brüning T. Müller O. Türk A. Schönhofer J. Mater. Chem. 1995 5 2167
- (1995) J. Mater. Chem. , vol.5 , pp. 2167
- Kuball, H.-G.¹ Brüning, H.² Müller, T.³ Türk, O.⁴ Schönhofer, A.⁵

20
- 0030883775
- H.-G. Kuball H. Brüning Chirality 1997 9 407
- (1997) Chirality , vol.9 , pp. 407
- Kuball, H.-G.¹ Brüning, H.²

21
- 0035801625
- R. A. van Delden B. L. Feringa Angew. Chem., Int. Ed. 2001 40 3198
- (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3198
- Van Delden, R.A.¹ Feringa, B.L.²

22
- 0013326146
- P. L. Rinaldi M. S. R. Naidu W. E. Conaway J. Org. Chem. 1982 47 3987
- (1982) J. Org. Chem. , vol.47 , pp. 3987
- Rinaldi, P.L.¹ Naidu, M.S.R.² Conaway, W.E.³

23
- 33845552509
- P. L. Rinaldi M. Wilk J. Org. Chem. 1983 48 2141
- (1983) J. Org. Chem. , vol.48 , pp. 2141
- Rinaldi, P.L.¹ Wilk, M.²

24
- 0037148060
- R. A. van Delden B. L. Feringa Chem. Commun. 2002 174
- (2002) Chem. Commun. , pp. 174
- Van Delden, R.A.¹ Feringa, B.L.²

25
- 4944220247
- R. Eelkema R. A. van Delden B. L. Feringa Angew. Chem., Int. Ed. 2004 43 5013
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5013
- Eelkema, R.¹ Van Delden, R.A.² Feringa, B.L.³

26
- 20444458271
- J. Yoshida H. Sato A. Yamagishi N. Hoshino J. Am. Chem. Soc. 2005 127 8453
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 8453
- Yoshida, J.¹ Sato, H.² Yamagishi, A.³ Hoshino, N.⁴

27
- 0037442343
- N. Hoshino Y. Matsuoka K. Okamoto A. Yamagishi J. Am. Chem. Soc. 2003 125 1718
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 1718
- Hoshino, N.¹ Matsuoka, Y.² Okamoto, K.³ Yamagishi, A.⁴

28
- 0037365350
- N. Anzai S. Machida K. Horie Liq. Cryst. 2003 30 359
- (2003) Liq. Cryst. , vol.30 , pp. 359
- Anzai, N.¹ MacHida, S.² Horie, K.³

29
- 0001502485
- G. Gottarelli G. P. Spada Mol. Cryst. Liq. Cryst. 1985 123 377
- (1985) Mol. Cryst. Liq. Cryst. , vol.123 , pp. 377
- Gottarelli, G.¹ Spada, G.P.²

30
- 0035808371
- TADDOL = α,α,α′,α′-tetraaryl-2,2- dimethyl-1,3-dioxolan-4,5-dimethanol; for a review see:
- S. Zahn G. Proni G. P. Spada J. W. Canary Chem.-Eur. J. 2001 7 88
- (2001) Chem.-Eur. J. , vol.7 , pp. 88
- Zahn, S.¹ Proni, G.² Spada, G.P.³ Canary, J.W.⁴

31
- 37649026114
- Nematic LC host ZLI-1695 is a eutectic mixture with a structure similar to ZLI-1167 (see Fig. 1) and n = 1, 2, 3, 6; phase transition temperatures were not available
- D. Seebach A. K. Beck A. Heckel Angew. Chem., Int. Ed. 2001 40 92
- (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 92
- Seebach, D.¹ Beck, A.K.² Heckel, A.³

32
- 0000330654
- H.-G. Kuball B. Weiss A. K. Beck D. Seebach Helv. Chim. Acta 1997 80 2507
- (1997) Helv. Chim. Acta , vol.80 , pp. 2507
- Kuball, H.-G.¹ Weiss, B.² Beck, A.K.³ Seebach, D.⁴

33
- 12844274397
- A. J. Seed M. E. Walsh J. W. Doane A. Khan Mol. Cryst. Liq. Cryst. 2004 410 201
- (2004) Mol. Cryst. Liq. Cryst. , vol.410 , pp. 201
- Seed, A.J.¹ Walsh, M.E.² Doane, J.W.³ Khan, A.⁴

34
- 0031025810
- C. Rosini G. P. Spada G. Proni S. Masiero S. Scamuzzi J. Am. Chem. Soc. 1997 119 506
- (1997) J. Am. Chem. Soc. , vol.119 , pp. 506
- Rosini, C.¹ Spada, G.P.² Proni, G.³ Masiero, S.⁴ Scamuzzi, S.⁵

35
- 0033603524
- S. Superchi M. I. Donnoli G. Proni G. P. Spada C. Rosini J. Org. Chem. 1999 64 4762
- (1999) J. Org. Chem. , vol.64 , pp. 4762
- Superchi, S.¹ Donnoli, M.I.² Proni, G.³ Spada, G.P.⁴ Rosini, C.⁵

36
- 33845373434
- G. Gottarelli G. P. Spada R. Bartsch G. Solladié R. G. Zimmermann J. Org. Chem. 1986 51 589
- (1986) J. Org. Chem. , vol.51 , pp. 589
- Gottarelli, G.¹ Spada, G.P.² Bartsch, R.³ Solladié, G.⁴ Zimmermann, R.G.⁵

37
- 0005166725
- G. Solladié G. Gottarelli Tetrahedron 1987 43 1425
- (1987) Tetrahedron , vol.43 , pp. 1425
- Solladié, G.¹ Gottarelli, G.²

38
- 4243818827
- The authors use M and P helicities when describing these systems, which is in conflict with IUPAC nomenclature. Therefore, these relative helicities will be designated pseudo-M (M′) and pseudo-P (P′) in this paper
- A. Ferrarini G. J. Moro P. L. Nordio Phys. Rev. E 1996 53 681
- (1996) Phys. Rev. e , vol.53 , pp. 681
- Ferrarini, A.¹ Moro, G.J.² Nordio, P.L.³

39
- 0020950101
- G. Gottarelli M. Hibert B. Samori G. Solladié G. P. Spada R. Zimmermann J. Am. Chem. Soc. 1983 105 7318
- (1983) J. Am. Chem. Soc. , vol.105 , pp. 7318
- Gottarelli, G.¹ Hibert, M.² Samori, B.³ Solladié, G.⁴ Spada, G.P.⁵ Zimmermann, R.⁶

40
- 0029082936
- C. Rosini I. Rosati G. P. Spada Chirality 1995 7 353
- (1995) Chirality , vol.7 , pp. 353
- Rosini, C.¹ Rosati, I.² Spada, G.P.³

41
- 3042995991
- H. J. Deussen P. V. Shibaev R. Vinokur T. Bjornholm K. Schaumburg K. Bechgaard V. P. Shibaev Liq. Cryst. 1996 21 327
- (1996) Liq. Cryst. , vol.21 , pp. 327
- Deussen, H.J.¹ Shibaev, P.V.² Vinokur, R.³ Bjornholm, T.⁴ Schaumburg, K.⁵ Bechgaard, K.⁶ Shibaev, V.P.⁷

42
- 0033950175
- M. Bandini S. Casolari P. G. Cozzi G. Proni E. Schmohel G. P. Spada E. Tagliavini A. U. Ronchi Eur. J. Org. Chem. 2000 491
- (2000) Eur. J. Org. Chem. , pp. 491
- Bandini, M.¹ Casolari, S.² Cozzi, P.G.³ Proni, G.⁴ Schmohel, E.⁵ Spada, G.P.⁶ Tagliavini, E.⁷ Ronchi, A.U.⁸

43
- 0033832988
- G. Proni G. P. Spada P. Lustenberger R. Welti F. Diederich J. Org. Chem. 2000 65 5522
- (2000) J. Org. Chem. , vol.65 , pp. 5522
- Proni, G.¹ Spada, G.P.² Lustenberger, P.³ Welti, R.⁴ Diederich, F.⁵

44
- 0000546092
- G. Gottarelli G. Proni G. P. Spada D. Fabbri S. Gladiali C. Rosini J. Org. Chem. 1996 61 2013
- (1996) J. Org. Chem. , vol.61 , pp. 2013
- Gottarelli, G.¹ Proni, G.² Spada, G.P.³ Fabbri, D.⁴ Gladiali, S.⁵ Rosini, C.⁶

45
- 0000972236
- G. Gottarelli G. P. Spada G. Solladié Nouv. J. Chim. 1986 10 691
- (1986) Nouv. J. Chim. , vol.10 , pp. 691
- Gottarelli, G.¹ Spada, G.P.² Solladié, G.³

46
- 0041297884
- V. E. Williams R. P. Lemieux Chem. Commun. 1996 2259
- (1996) Chem. Commun. , pp. 2259
- Williams, V.E.¹ Lemieux, R.P.²

47
- 0034812111
- A. di Matteo S. M. Todd G. Gottarelli G. Solladié V. E. Williams R. P. Lemieux A. Ferrarini G. P. Spada J. Am. Chem. Soc. 2001 123 7842
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 7842
- Di Matteo, A.¹ Todd, S.M.² Gottarelli, G.³ Solladié, G.⁴ Williams, V.E.⁵ Lemieux, R.P.⁶ Ferrarini, A.⁷ Spada, G.P.⁸

48
- 25844461768
- R. Eelkema B. L. Feringa J. Am. Chem. Soc. 2005 127 13480
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 13480
- Eelkema, R.¹ Feringa, B.L.²

49
- 33645926367
- R. Eelkema B. L. Feringa Org. Lett. 2006 8 1331
- (2006) Org. Lett. , vol.8 , pp. 1331
- Eelkema, R.¹ Feringa, B.L.²

50
- 84987584115
- G. Gottarelli H.-J. Hansen G. P. Spada R. H. Weber Helv. Chim. Acta 1987 70 430
- (1987) Helv. Chim. Acta , vol.70 , pp. 430
- Gottarelli, G.¹ Hansen, H.-J.² Spada, G.P.³ Weber, R.H.⁴

51
- 84986384792
- W. Bernhard P. Brügger J. J. Daly G. Englert P. Schönholzer H.-J. Hansen Helv. Chim. Acta 1985 68 415
- (1985) Helv. Chim. Acta , vol.68 , pp. 415
- Bernhard, W.¹ Brügger, P.² Daly, J.J.³ Englert, G.⁴ Schönholzer, P.⁵ Hansen, H.-J.⁶

52
- 4444300394
- R. Holzwarth R. Bartsch Z. Cherkaoui G. Solladié Chem.-Eur. J. 2004 10 3931
- (2004) Chem.-Eur. J. , vol.10 , pp. 3931
- Holzwarth, R.¹ Bartsch, R.² Cherkaoui, Z.³ Solladié, G.⁴

53
- 23944489682
- The molecular structure of LC host ROTN 3010 is unavailable
- R. Holzwarth R. Bartsch Z. Cherkaoui G. Solladié Eur. J. Org. Chem. 2005 3536
- (2005) Eur. J. Org. Chem. , pp. 3536
- Holzwarth, R.¹ Bartsch, R.² Cherkaoui, Z.³ Solladié, G.⁴

54
- 84950914830
- G. Heppke D. Lötzsch F. Oestreicher Z. Naturforsch. 1986 41a 1214
- (1986) Z. Naturforsch. , vol.41 , pp. 1214
- Heppke, G.¹ Lötzsch, D.² Oestreicher, F.³

55
- 0032573485
- K. Akagi G. Piao S. Kaneko K. Sakamaki H. Shirakawa M. Kyotani Science 1998 282 1683
- (1998) Science , vol.282 , pp. 1683
- Akagi, K.¹ Piao, G.² Kaneko, S.³ Sakamaki, K.⁴ Shirakawa, H.⁵ Kyotani, M.⁶

56
- 22144485640
- T. Mori T. Sato M. Kyotani K. Akagi Synth. Met. 2003 135-136 83
- (2003) Synth. Met. , vol.135-136 , pp. 83
- Mori, T.¹ Sato, T.² Kyotani, M.³ Akagi, K.⁴

57
- 12344281574
- K. Kanazawa I. Higuchi K. Akagi Mol. Cryst. Liq. Cryst. 2001 364 825
- (2001) Mol. Cryst. Liq. Cryst. , vol.364 , pp. 825
- Kanazawa, K.¹ Higuchi, I.² Akagi, K.³

58
- 1542496520
- Special issue of Scientific American: Nanotech, The Science of the Small Gets Down to Business, September 2001 For reviews, see:
- J. Cheung L. D. Field S. Sternhell J. Org. Chem. 1997 62 7044
- (1997) J. Org. Chem. , vol.62 , pp. 7044
- Cheung, J.¹ Field, L.D.² Sternhell, S.³

59
- 0034596923
- V. Balzani A. Credi F. M. Raymo J. F. Stoddart Angew. Chem., Int. Ed. 2000 39 3348
- (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3348
- Balzani, V.¹ Credi, A.² Raymo, F.M.³ Stoddart, J.F.⁴

60
- 33644910136
- B. L. Feringa, Wiley-VCH, Weinheim, The May 2000 issue of Chem. Rev., Memories and Switches
- Molecular Switches, ed., B. L. Feringa, Wiley-VCH, Weinheim, 2001
- (2001) Molecular Switches, Ed.

61
- 0004256338
- Elsevier, Amsterdam, Selected examples:
- F. L. Carter, H. Siatkowski and H. Wohltgen, Molecular Electronic Devices, Elsevier, Amsterdam, 1988
- (1988) Molecular Electronic Devices
- Carter, F.L.¹ Siatkowski, H.² Wohltgen, H.³

62
- 0035052525
- M. Moriyama S. Song H. Matsuda N. Tamaoki J. Mater. Chem. 2001 11 1003
- (2001) J. Mater. Chem. , vol.11 , pp. 1003
- Moriyama, M.¹ Song, S.² Matsuda, H.³ Tamaoki, N.⁴

63
- 0032511670
- S. Kurihara T. Kanda T. Nagase T. Nonaka Appl. Phys. Lett. 1998 73 2081
- (1998) Appl. Phys. Lett. , vol.73 , pp. 2081
- Kurihara, S.¹ Kanda, T.² Nagase, T.³ Nonaka, T.⁴

64
- 0033640039
- N. Tamaoki S. Song M. Moriyama H. Matsuda Adv. Mater. 2000 12 94
- (2000) Adv. Mater. , vol.12 , pp. 94
- Tamaoki, N.¹ Song, S.² Moriyama, M.³ Matsuda, H.⁴

65
- 0036157764
- S. V. Serak E. O. Arikainen H. F. Gleeson V. A. Grozhik J.-P. Guillou N. A. Usova Liq. Cryst. 2002 29 19
- (2002) Liq. Cryst. , vol.29 , pp. 19
- Serak, S.V.¹ Arikainen, E.O.² Gleeson, H.F.³ Grozhik, V.A.⁴ Guillou, J.-P.⁵ Usova, N.A.⁶

66
- 0001930425
- S. Tazuke S. Kurihara T. Ikeda Chem. Lett. 1987 911
- (1987) Chem. Lett. , pp. 911
- Tazuke, S.¹ Kurihara, S.² Ikeda, T.³

67
- 0004942710
- E48 is a nematic mixture of cyanobiphenyls, similar to E7. The exact composition and phase transition temperatures are not available
- E. Sackmann J. Am. Chem. Soc. 1971 93 7088
- (1971) J. Am. Chem. Soc. , vol.93 , pp. 7088
- Sackmann, E.¹

68
- 31944435588
- C. Ruslim M. Nakagawa S. Morino K. Ichimura Mol. Cryst. Liq. Cryst. 2001 365 55
- (2001) Mol. Cryst. Liq. Cryst. , vol.365 , pp. 55
- Ruslim, C.¹ Nakagawa, M.² Morino, S.³ Ichimura, K.⁴

69
- 4644327951
- T. Yoshioka M. D. Z. Alam T. Ogata T. Nonaka S. Kurihara Liq. Cryst. 2004 31 1285
- (2004) Liq. Cryst. , vol.31 , pp. 1285
- Yoshioka, T.¹ Alam, M.D.Z.² Ogata, T.³ Nonaka, T.⁴ Kurihara, S.⁵

70
- 0033807611
- S. Kurihara S. Nomiyama T. Nonaka Chem. Mater. 2000 12 9
- (2000) Chem. Mater. , vol.12 , pp. 9
- Kurihara, S.¹ Nomiyama, S.² Nonaka, T.³

71
- 0034852211
- S. Kurihara S. Nomiyama T. Nonaka Chem. Mater. 2001 13 1992
- (2001) Chem. Mater. , vol.13 , pp. 1992
- Kurihara, S.¹ Nomiyama, S.² Nonaka, T.³

72
- 0034224541
- C. Ruslim K. Ichimura J. Phys. Chem. B 2000 104 6529
- (2000) J. Phys. Chem. B , vol.104 , pp. 6529
- Ruslim, C.¹ Ichimura, K.²

73
- 0347719289
- R. A. van Delden T. Mecca C. Rosini B. L. Feringa Chem.-Eur. J. 2004 10 61
- (2004) Chem.-Eur. J. , vol.10 , pp. 61
- Van Delden, R.A.¹ Mecca, T.² Rosini, C.³ Feringa, B.L.⁴

74
- 0037424032
- S. Pieraccini S. Masiero G. P. Spada G. Gottarelli Chem. Commun. 2003 598
- (2003) Chem. Commun. , pp. 598
- Pieraccini, S.¹ Masiero, S.² Spada, G.P.³ Gottarelli, G.⁴

75
- 9244252482
- Nematic LC host Phase 1052 is a mixture with a structure similar to ZLI-389 (see Fig. 1). The exact composition and phase transition temperatures are not available
- S. Pieraccini G. Gottarelli R. Labruto S. Masiero O. Pandoli G. P. Spada Chem.-Eur. J. 2004 10 5632
- (2004) Chem.-Eur. J. , vol.10 , pp. 5632
- Pieraccini, S.¹ Gottarelli, G.² Labruto, R.³ Masiero, S.⁴ Pandoli, O.⁵ Spada, G.P.⁶

76
- 0035138660
- C. Ruslim K. Ichimura Adv. Mater. 2001 13 37
- (2001) Adv. Mater. , vol.13 , pp. 37
- Ruslim, C.¹ Ichimura, K.²

77
- 0036928505
- E44 is a nematic mixture of cyanobiphenyls, similar to E7; DON-103 is a nematic mixture of cyclohexanecarboxylic acid phenyl esters
- C. Ruslim K. Ichimura J. Mater. Chem. 2002 12 3377
- (2002) J. Mater. Chem. , vol.12 , pp. 3377
- Ruslim, C.¹ Ichimura, K.²

78
- 0034248554
- H.-K. Lee K. Doi H. Harada O. Tsutsumi A. Kanazawa T. Shiono T. Ikeda J. Phys. Chem. B 2000 104 7023
- (2000) J. Phys. Chem. B , vol.104 , pp. 7023
- Lee, H.-K.¹ Doi, K.² Harada, H.³ Tsutsumi, O.⁴ Kanazawa, A.⁵ Shiono, T.⁶ Ikeda, T.⁷

79
- 0034246863
- Nematic LC host ZLI-2359 is a mixture with a structure similar to ZLI-1167 (see Fig. 1). The exact composition and phase transition temperatures are not available Due to overlap in the absorption spectra of the E and Z isomers, no complete conversion of one isomer to the other can be achieved by irradiation. As a result of this, the helical twisting powers of the photostationary states (PSS) are reported. Moreover, the presence of two azobenzene moieties makes the PSS composition even more complex
- A. Y. Bobrovsky N. I. Boiko V. P. Shibaev J. Springer Adv. Mater. 2000 12 1180
- (2000) Adv. Mater. , vol.12 , pp. 1180
- Bobrovsky, A.Y.¹ Boiko, N.I.² Shibaev, V.P.³ Springer, J.⁴

80
- 0347248506
- P. M. A. Bonaccorsi D. A. Dunmur J. F. Stoddart New J. Chem. 1988 12 83
- (1988) New J. Chem. , vol.12 , pp. 83
- Bonaccorsi, P.M.A.¹ Dunmur, D.A.² Stoddart, J.F.³

81
- 0001233991
- S. N. Yarmolenko L. A. Kutulya V. V. Vashchenko L. V. Chepeleva Liq. Cryst. 1994 16 877
- (1994) Liq. Cryst. , vol.16 , pp. 877
- Yarmolenko, S.N.¹ Kutulya, L.A.² Vashchenko, V.V.³ Chepeleva, L.V.⁴

82
- 0032304739
- M. Brehmer J. Lub P. van de Witte Adv. Mater. 1998 10 1438
- (1998) Adv. Mater. , vol.10 , pp. 1438
- Brehmer, M.¹ Lub, J.² Van De Witte, P.³

83
- 0348080703
- M. Irie Chem. Rev. 2000 100 1685
- (2000) Chem. Rev. , vol.100 , pp. 1685
- Irie, M.¹

84
- 0032184275
- C. Denekamp B. L. Feringa Adv. Mater. 1998 10 1080
- (1998) Adv. Mater. , vol.10 , pp. 1080
- Denekamp, C.¹ Feringa, B.L.²

85
- 0033803574
- T. Yamaguchi T. Inagawa H. Nakazumi S. Irie M. Irie Chem. Mater. 2000 12 869
- (2000) Chem. Mater. , vol.12 , pp. 869
- Yamaguchi, T.¹ Inagawa, T.² Nakazumi, H.³ Irie, S.⁴ Irie, M.⁵

86
- 1842871097
- T. Yamaguchi T. Inagawa H. Nakazumi S. Irie M. Irie Mol. Cryst. Liq. Cryst. 2001 365 861
- (2001) Mol. Cryst. Liq. Cryst. , vol.365 , pp. 861
- Yamaguchi, T.¹ Inagawa, T.² Nakazumi, H.³ Irie, S.⁴ Irie, M.⁵

87
- 0034478748
- T. Yamaguchi T. Inagawa H. Nakazumi S. Irie M. Irie Mol. Cryst. Liq. Cryst. 2000 345 287
- (2000) Mol. Cryst. Liq. Cryst. , vol.345 , pp. 287
- Yamaguchi, T.¹ Inagawa, T.² Nakazumi, H.³ Irie, S.⁴ Irie, M.⁵

88
- 0034777230
- T. Yamaguchi T. Inagawa H. Nakazumi S. Irie M. Irie J. Mater. Chem. 2001 11 2453
- (2001) J. Mater. Chem. , vol.11 , pp. 2453
- Yamaguchi, T.¹ Inagawa, T.² Nakazumi, H.³ Irie, S.⁴ Irie, M.⁵

89
- 0001765706
- Y. Yokoyama Chem. Rev. 2000 100 1717
- (2000) Chem. Rev. , vol.100 , pp. 1717
- Yokoyama, Y.¹

90
- 0031496568
- Y. Yokoyama T. Sagisaka Chem. Lett. 1997 687
- (1997) Chem. Lett. , pp. 687
- Yokoyama, Y.¹ Sagisaka, T.²

91
- 0033979201
- T. Sagisaka Y. Yokoyama Bull. Chem. Soc. Jpn. 2000 73 191
- (2000) Bull. Chem. Soc. Jpn. , vol.73 , pp. 191
- Sagisaka, T.¹ Yokoyama, Y.²

92
- 0003942864
- Wiley, New York
- For stereochemical definitions, see: E. L. Eliel and S. H. Wilen, Stereochemistry of Organic Compounds, Wiley, New York, 1994
- (1994) Stereochemistry of Organic Compounds
- Eliel, E.L.¹ Wilen, S.H.²

93
- 0000578298
- B. L. Feringa N. P. M. Huck H. A. van Doren J. Am. Chem. Soc. 1995 117 9929
- (1995) J. Am. Chem. Soc. , vol.117 , pp. 9929
- Feringa, B.L.¹ Huck, N.P.M.² Van Doren, H.A.³

94
- 33749566179
- PhD Thesis, University of Groningen, Nematic LC host M15 is 4′-pentyloxybiphenylnitrile, with C-N and N-I transition temperatures of 48 and 67 °C, respectively
- N. P. M. Huck, PhD Thesis, University of Groningen, 1997
- (1997)
- Huck, N.P.M.¹

95
- 0038395985
- R. A. van Delden M. B. van Gelder N. P. M. Huck B. L. Feringa Adv. Funct. Mater. 2003 13 319
- (2003) Adv. Funct. Mater. , vol.13 , pp. 319
- Van Delden, R.A.¹ Van Gelder, M.B.² Huck, N.P.M.³ Feringa, B.L.⁴

96
- 33749569379
- PhD Thesis, University of Groningen
- R. A. van Delden, PhD Thesis, University of Groningen, 2002
- (2002)
- Van Delden, R.A.¹

97
- 0034675016
- C.-T. Chen Y.-C. Chou J. Am. Chem. Soc. 2000 122 7662
- (2000) J. Am. Chem. Soc. , vol.122 , pp. 7662
- Chen, C.-T.¹ Chou, Y.-C.²

98
- 0033539072
- N. Koumura R. W. J. Zijlstra R. A. van Delden N. Harada B. L. Feringa Nature 1999 401 152
- (1999) Nature , vol.401 , pp. 152
- Koumura, N.¹ Zijlstra, R.W.J.² Van Delden, R.A.³ Harada, N.⁴ Feringa, B.L.⁵

99
- 0037117620
- R. A. van Delden N. Koumura N. Harada B. L. Feringa Proc. Natl. Acad. Sci. U. S. A. 2002 99 4945
- (2002) Proc. Natl. Acad. Sci. U. S. A. , vol.99 , pp. 4945
- Van Delden, R.A.¹ Koumura, N.² Harada, N.³ Feringa, B.L.⁴

100
- 33749161227
- 10.1002/asia.200600116
- R. Eelkema B. L. Feringa Chem. Asian J. 2006 10.1002/asia.200600116
- (2006) Chem. Asian J.
- Eelkema, R.¹ Feringa, B.L.²

101
- 33644865048
- Exceptions to the rule can be found among certain photoactive chiral chromium complexes, see for instance:
- R. Eelkema M. M. Pollard J. Vicario N. Katsonis B. Serrano Ramon C. W. M. Bastiaansen D. J. Broer B. L. Feringa Nature 2006 440 163
- (2006) Nature , vol.440 , pp. 163
- Eelkema, R.¹ Pollard, M.M.² Vicario, J.³ Katsonis, N.⁴ Serrano Ramon, B.⁵ Bastiaansen, C.W.M.⁶ Broer, D.J.⁷ Feringa, B.L.⁸

102
- 0001228352
- K. L. Stevenson J. F. Verdieck J. Am. Chem. Soc. 1968 90 2974
- (1968) J. Am. Chem. Soc. , vol.90 , pp. 2974
- Stevenson, K.L.¹ Verdieck, J.F.²

103
- 10144261883
- N. P. M. Huck W. F. Jager B. de Lange B. L. Feringa Science 1996 273 1686
- (1996) Science , vol.273 , pp. 1686
- Huck, N.P.M.¹ Jager, W.F.² De Lange, B.³ Feringa, B.L.⁴

104
- 0001268014
- M. Suarez G. B. Schuster J. Am. Chem. Soc. 1995 117 6732
- (1995) J. Am. Chem. Soc. , vol.117 , pp. 6732
- Suarez, M.¹ Schuster, G.B.²

105
- 0001042238
- Y. Zhang G. B. Schuster J. Am. Chem. Soc. 1994 116 4852
- (1994) J. Am. Chem. Soc. , vol.116 , pp. 4852
- Zhang, Y.¹ Schuster, G.B.²

106
- 0028807720
- Y. Zhang G. B. Schuster J. Org. Chem. 1995 60 7192
- (1995) J. Org. Chem. , vol.60 , pp. 7192
- Zhang, Y.¹ Schuster, G.B.²

107
- 0001973515
- R. Lemieux G. B. Schuster J. Org. Chem. 1993 58 100
- (1993) J. Org. Chem. , vol.58 , pp. 100
- Lemieux, R.¹ Schuster, G.B.²

108
- 33751386157
- B. S. Udayakumar G. B. Schuster J. Org. Chem. 1993 58 4165
- (1993) J. Org. Chem. , vol.58 , pp. 4165
- Udayakumar, B.S.¹ Schuster, G.B.²

109
- 0001460607
- Y. Zhang G. B. Schuster J. Org. Chem. 1994 59 1855
- (1994) J. Org. Chem. , vol.59 , pp. 1855
- Zhang, Y.¹ Schuster, G.B.²

110
- 0033520734
- K. S. Burnham G. B. Schuster J. Am. Chem. Soc. 1999 121 10245
- (1999) J. Am. Chem. Soc. , vol.121 , pp. 10245
- Burnham, K.S.¹ Schuster, G.B.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.