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Shimbo, Y.6
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Takezoe, H.11
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33747171975
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K. Nishida M. Cepic W. J. Kim S. K. Lee S. Heo J. G. Lee T. Takahashi K. Ishikawa K.-T. Kang J. Watanabe H. Takezoe Phys. Rev. E. 2006 74 021704
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90
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34547737386
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This value is obtained from an average lateral distance between the molecules of 0.45 nm assuming a stacking in the bend direction of the molecules with a bend angle of 120°
-
This value is obtained from an average lateral distance between the molecules of 0.45 nm assuming a stacking in the bend direction of the molecules with a bend angle of 120°
-
-
-
-
97
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0042823831
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-
Field induced dark conglomerate phases:
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D. A. Coleman J. Fernsler N. Chattham M. Nakata Y. Takanishi E. Korblova D. R. Link R.-F. Shao W. G. Jang J. E. Maclennan O. Mondainn-Monval C. Boyer W. Weissflog G. Pelzl L.-C. Chien J. Zasadzinski J. Watanabe D. M. Walba H. Takezoe N. A. Clark Science 2003 301 1204
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Coleman, D.A.1
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Link, D.R.7
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MacLennan, J.E.10
Mondainn-Monval, O.11
Boyer, C.12
Weissflog, W.13
Pelzl, G.14
Chien, L.-C.15
Zasadzinski, J.16
Watanabe, J.17
Walba, D.M.18
Takezoe, H.19
Clark, N.A.20
more..
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100
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34547751312
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The molecular length measured with CPK models (space filling molecular models according to Corey, Pauling and Koltum) assuming a V-shaped conformation with an opening angle of 120° and alkyl chains in the all-trans conformation is L = 6.2 nm. The difference to the effective molecular length results from chain-melting and partial intercalation of the alkyl chains of adjacent layers
-
The molecular length measured with CPK models (space filling molecular models according to Corey, Pauling and Koltum) assuming a V-shaped conformation with an opening angle of 120° and alkyl chains in the all-trans conformation is L = 6.2 nm. The difference to the effective molecular length results from chain-melting and partial intercalation of the alkyl chains of adjacent layers
-
-
-
-
101
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-
34547740017
-
-
In this case, in principle there could be diastereomeric relations between helix sense, layer chirality and molecular conformational chirality, which contribute to the transfer of chirality
-
In this case, in principle there could be diastereomeric relations between helix sense, layer chirality and molecular conformational chirality, which contribute to the transfer of chirality
-
-
-
-
105
-
-
34547737904
-
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S.-W. Choi K. Fukuda S. Nakahara K. Kishikawa Y. Takanishi K. Ishikawa J. Watanabe H. Takezoe Chem. Lett. 2006 35 1171
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, pp. 1171
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Choi, S.-W.1
Fukuda, K.2
Nakahara, S.3
Kishikawa, K.4
Takanishi, Y.5
Ishikawa, K.6
Watanabe, J.7
Takezoe, H.8
-
106
-
-
34547733940
-
-
Indexing is not unique, from the X-ray results alone. There is, for instance, a very plausible oblique interpretation with a = 9.2 nm, b = 5.37 nm, and γ = 100°, which would also give an undulated layer structure, but with tilted molecules. Since the texture observed by polarizing microscopy suggests a non-tilted or anticlinic tilted arrangement of the molecules, and because a non-tilted or anticlinic tilted organization in an oblique lattice is unlikely, we prefer the rectangular version with non-tilted molecules
-
Indexing is not unique, from the X-ray results alone. There is, for instance, a very plausible oblique interpretation with a = 9.2 nm, b = 5.37 nm, and γ = 100°, which would also give an undulated layer structure, but with tilted molecules. Since the texture observed by polarizing microscopy suggests a non-tilted or anticlinic tilted arrangement of the molecules, and because a non-tilted or anticlinic tilted organization in an oblique lattice is unlikely, we prefer the rectangular version with non-tilted molecules
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