-
6
-
-
79953717403
-
-
X. C. Chen H. M. Chen C. Tripisciano A. Jedrzejewska M. H. Rummeli R. Klingeler R. J. Kalenczuk P. K. Chu E. Borowiak-Palen Chem.-Eur. J. 2011 17 4454
-
(2011)
Chem.-Eur. J.
, vol.17
, pp. 4454
-
-
Chen, X.C.1
Chen, H.M.2
Tripisciano, C.3
Jedrzejewska, A.4
Rummeli, M.H.5
Klingeler, R.6
Kalenczuk, R.J.7
Chu, P.K.8
Borowiak-Palen, E.9
-
17
-
-
49149087482
-
-
S. D. Bergin V. Nicolosi P. V. Streich S. Giordani Z. Y. Sun A. H. Windle P. Ryan N. P. P. Niraj Z. T. T. Wang L. Carpenter W. J. Blau J. J. Boland J. P. Hamilton J. N. Coleman Adv. Mater. 2008 20 1876
-
(2008)
Adv. Mater.
, vol.20
, pp. 1876
-
-
Bergin, S.D.1
Nicolosi, V.2
Streich, P.V.3
Giordani, S.4
Sun, Z.Y.5
Windle, A.H.6
Ryan, P.7
Niraj, N.P.P.8
Wang, Z.T.T.9
Carpenter, L.10
Blau, W.J.11
Boland, J.J.12
Hamilton, J.P.13
Coleman, J.N.14
-
19
-
-
0036919989
-
-
S. Niyogi M. A. Hamon H. Hu B. Zhao P. Bhowmik R. Sen M. E. Itkis R. C. Haddon Acc. Chem. Res. 2002 35 1105
-
(2002)
Acc. Chem. Res.
, vol.35
, pp. 1105
-
-
Niyogi, S.1
Hamon, M.A.2
Hu, H.3
Zhao, B.4
Bhowmik, P.5
Sen, R.6
Itkis, M.E.7
Haddon, R.C.8
-
23
-
-
84885855292
-
-
We used the phrasing "semi-aromatic" about the present nanotube, where aromatic moieties are inserted in between aliphatic moieties, to distinguish it from aromatic nanotubes being fully aromatic from one end to another such as in MWNTs and SWNTs. This phrasing has been used by Shabanian when describing aliphatic-aromatic polyamides, see
-
T. Wixe C.-J. Wallentin M. T. Johnson P. Fristrup S. Lidin K. Wärnmark Chem.-Eur. J. 2013 19 14963
-
(2013)
Chem.-Eur. J.
, vol.19
, pp. 14963
-
-
Wixe, T.1
Wallentin, C.-J.2
Johnson, M.T.3
Fristrup, P.4
Lidin, S.5
Wärnmark, K.6
-
27
-
-
84908366450
-
-
Diamond-Crystal and Molecular Structure Visualization Crystal Impact-Dr. H. Putz & Dr. K. Brandenburg GbR, Kreuzherrenstr. 102, 53227 Bonn, Germany
-
Diamond-Crystal and Molecular Structure Visualization Crystal Impact-Dr. H. Putz & Dr. K. Brandenburg GbR, Kreuzherrenstr. 102, 53227 Bonn, Germany http://www.crystalimpact.com/diamond
-
-
-
-
28
-
-
67449126480
-
-
S. Ding L. Jia A. Durandin C. Crean A. Kolbanovskiy V. Shafirovich S. Broyde N. E. Geacintov Chem. Res. Toxicol. 2009 22 1189
-
(2009)
Chem. Res. Toxicol.
, vol.22
, pp. 1189
-
-
Ding, S.1
Jia, L.2
Durandin, A.3
Crean, C.4
Kolbanovskiy, A.5
Shafirovich, V.6
Broyde, S.7
Geacintov, N.E.8
-
34
-
-
84894347175
-
-
Schrödinger, LLC, New York, NY
-
Schrödinger Release 2013-1: Maestro, version 9.4, Schrödinger, LLC, New York, NY, 2013
-
(2013)
Schrödinger Release 2013-1: Maestro, Version 9.4
-
-
-
38
-
-
0004093092
-
-
in, ed. H.-J. Schneider and H. Dürr, VCH, Weinheim, Federal Republic of Germany, New York, 123-143
-
C. S. Wilcox, in Frontiers in supramolecular organic chemistry and photochemistry, ed., H.-J. Schneider, and, H. Dürr, VCH, Weinheim, Federal Republic of Germany, New York, 1991, pp. 123-143
-
(1991)
Frontiers in Supramolecular Organic Chemistry and Photochemistry
-
-
Wilcox, C.S.1
-
40
-
-
84906270337
-
-
Schrödinger, LLC, New York, NY
-
Schrödinger Release 2013-3: Maestro, version 9.6, Schrödinger, LLC, New York, NY, 2013
-
(2013)
Schrödinger Release 2013-3: Maestro, Version 9.6
-
-
-
41
-
-
84908373057
-
-
Schrödinger, LLC, New York, NY
-
MacroModel, Schrödinger Release 2013-3: MacroModel, version 10.2, Schrödinger, LLC, New York, NY, 2013
-
(2013)
MacroModel, Schrödinger Release 2013-3: MacroModel, Version 10.2
-
-
-
42
-
-
25144517646
-
-
J. L. Banks H. S. Beard Y. Cao A. E. Cho W. Damm R. Farid A. K. Felts T. A. Halgren D. T. Mainz J. R. Maple R. Murphy D. M. Philipp M. P. Repasky L. Y. Zhang B. J. Berne R. A. Friesner E. Gallicchio R. M. Levy J. Comput. Chem. 2005 26 1752
-
(2005)
J. Comput. Chem.
, vol.26
, pp. 1752
-
-
Banks, J.L.1
Beard, H.S.2
Cao, Y.3
Cho, A.E.4
Damm, W.5
Farid, R.6
Felts, A.K.7
Halgren, T.A.8
Mainz, D.T.9
Maple, J.R.10
Murphy, R.11
Philipp, D.M.12
Repasky, M.P.13
Zhang, L.Y.14
Berne, B.J.15
Friesner, R.A.16
Gallicchio, E.17
Levy, R.M.18
-
43
-
-
84908366449
-
-
http://www.schrodinger.com/kb/1006
-
-
-
-
53
-
-
25144517646
-
-
J. L. Banks H. S. Beard Y. Cao A. E. Cho W. Damm R. Farid A. K. Felts T. A. Halgren D. T. Mainz J. R. Maple R. Murphy D. M. Philipp M. P. Repasky L. Y. Zhang B. J. Berne R. A. Friesner E. Gallicchio R. M. Levy J. Comput. Chem. 2005 26 1752
-
(2005)
J. Comput. Chem.
, vol.26
, pp. 1752
-
-
Banks, J.L.1
Beard, H.S.2
Cao, Y.3
Cho, A.E.4
Damm, W.5
Farid, R.6
Felts, A.K.7
Halgren, T.A.8
Mainz, D.T.9
Maple, J.R.10
Murphy, R.11
Philipp, D.M.12
Repasky, M.P.13
Zhang, L.Y.14
Berne, B.J.15
Friesner, R.A.16
Gallicchio, E.17
Levy, R.M.18
-
56
-
-
79959190033
-
-
Gaussian, Inc., Wallingford, CT
-
M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, Ö. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski and D. J. Fox, Gaussian 09, Revision D.01, Gaussian, Inc., Wallingford, CT, 2009
-
(2009)
Gaussian 09, Revision D.01
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Scalmani, G.7
Barone, V.8
Mennucci, B.9
Petersson, G.A.10
Nakatsuji, H.11
Caricato, M.12
Li, X.13
Hratchian, H.P.14
Izmaylov, A.F.15
Bloino, J.16
Zheng, G.17
Sonnenberg, J.L.18
Hada, M.19
Ehara, M.20
Toyota, K.21
Fukuda, R.22
Hasegawa, J.23
Ishida, M.24
Nakajima, T.25
Honda, Y.26
Kitao, O.27
Nakai, H.28
Vreven, T.29
Montgomery, J.A.30
Peralta, J.E.31
Ogliaro, F.32
Bearpark, M.33
Heyd, J.J.34
Brothers, E.35
Kudin, K.N.36
Staroverov, V.N.37
Kobayashi, R.38
Normand, J.39
Raghavachari, K.40
Rendell, A.41
Burant, J.C.42
Iyengar, S.S.43
Tomasi, J.44
Cossi, M.45
Rega, N.46
Millam, J.M.47
Klene, M.48
Knox, J.E.49
Cross, J.B.50
Bakken, V.51
Adamo, C.52
Jaramillo, J.53
Gomperts, R.54
Stratmann, R.E.55
Yazyev, O.56
Austin, A.J.57
Cammi, R.58
Pomelli, C.59
Ochterski, J.W.60
Martin, R.L.61
Morokuma, K.62
Zakrzewski, V.G.63
Voth, G.A.64
Salvador, P.65
Dannenberg, J.J.66
Dapprich, S.67
Daniels, A.D.68
Farkas Ö.69
Foresman, J.B.70
Ortiz, J.V.71
Cioslowski, J.72
Fox, D.J.73
more..
-
59
-
-
84962349001
-
-
Comprehensive Chiroptical Spectroscopy: Applications in Stereochemical Analysis of Synthetic Compounds, Natural Products, and Biomolecules, Volume 2
-
M. Cossi N. Rega G. Scalmani V. Barone J. Comput. Chem. 2003 24 669
-
(2003)
J. Comput. Chem.
, vol.24
, pp. 669
-
-
Cossi, M.1
Rega, N.2
Scalmani, G.3
Barone, V.4
-
62
-
-
67650847297
-
-
Institute of Physics, Academy of Sciences of the Czech Republic
-
V. Petricek, L. Palatinus and M. Dusek, JANA 2006, Institute of Physics, Academy of Sciences of the Czech Republic, 2006
-
(2006)
JANA 2006
-
-
Petricek, V.1
Palatinus, L.2
Dusek, M.3
|