-
5
-
-
79956003949
-
-
D. Pisignano M. Anni G. Gigli R. Cingolani M. Zavelani-Rossi G. Lanzani G. Barbarella L. Favaretto Appl. Phys. Lett. 2002 81 3534 3536
-
(2002)
Appl. Phys. Lett.
, vol.81
, pp. 3534-3536
-
-
Pisignano, D.1
Anni, M.2
Gigli, G.3
Cingolani, R.4
Zavelani-Rossi, M.5
Lanzani, G.6
Barbarella, G.7
Favaretto, L.8
-
8
-
-
77955211085
-
-
F. Jäkle Chem. Rev. 2010 110 3985 4022
-
(2010)
Chem. Rev.
, vol.110
, pp. 3985-4022
-
-
Jäkle, F.1
-
9
-
-
20944433003
-
-
references cited herein
-
G. Yu S. Yin Y. Liu J. Chen X. Xu X. Sun D. Ma X. Zhan Q. Peng Z. Shuai B. Tang D. Zhu W. Fang Y. Luo J. Am. Chem. Soc. 2005 127 6335 6346
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6335-6346
-
-
Yu, G.1
Yin, S.2
Liu, Y.3
Chen, J.4
Xu, X.5
Sun, X.6
Ma, D.7
Zhan, X.8
Peng, Q.9
Shuai, Z.10
Tang, B.11
Zhu, D.12
Fang, W.13
Luo, Y.14
-
24
-
-
0034674925
-
-
The following reviews provide more detailed insight into optical, electronic and sensory applications of organoboranes.
-
H. E. Katz J. Johnson A. J. Lovinger W. Li J. Am. Chem. Soc. 2000 122 7787 7792
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7787-7792
-
-
Katz, H.E.1
Johnson, J.2
Lovinger, A.J.3
Li, W.4
-
36
-
-
70349782095
-
-
A. Lorbach M. Bolte H. Li H.-W. Lerner M. C. Holthausen F. Jäkle M. Wagner Angew. Chem., Int. Ed. 2009 48 4584 4588
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 4584-4588
-
-
Lorbach, A.1
Bolte, M.2
Li, H.3
Lerner, H.-W.4
Holthausen, M.C.5
Jäkle, F.6
Wagner, M.7
-
47
-
-
77955063465
-
-
C. Bresner C. J. E. Haynes D. A. Addy A. E. J. Broomsgrove P. Fitzpatrick D. Vidovic A. L. Thompson I. A. Fallis S. Aldridge New J. Chem. 2010 34 1652 1659
-
(2010)
New J. Chem.
, vol.34
, pp. 1652-1659
-
-
Bresner, C.1
Haynes, C.J.E.2
Addy, D.A.3
Broomsgrove, A.E.J.4
Fitzpatrick, P.5
Vidovic, D.6
Thompson, A.L.7
Fallis, I.A.8
Aldridge, S.9
-
51
-
-
84870502599
-
-
We have prepared the unsubstituted species 9,10-diphenyl-DBA, 9,10-bis(1′-naphthyl)-DBA and 9,10-bis(9′-anthryl)-DBA and found only negligible differences in their optoelectronic properties compared to 2a-c. However, because of higher sensitivity to air and moisture or pure solubility in all common solvents, analytically pure samples could not be obtained. We therefore restrict our discussion to 2a-c A six-step synthesis protocol together with an X-ray crystal structure analysis of 2a has already been described (i.e. 2a*)
-
C. Dou S. Saito K. Matsuo I. Hisaki S. Yamaguchi Angew. Chem., Int. Ed. 2012 51 12206 12210
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 12206-12210
-
-
Dou, C.1
Saito, S.2
Matsuo, K.3
Hisaki, I.4
Yamaguchi, S.5
-
52
-
-
78549292422
-
-
8, which we require for comparison, and the X-ray crystal structure analysis of a polymorph
-
T. Agou M. Sekine T. Kawashima Tetrahedron Lett. 2010 51 5013 5015
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 5013-5015
-
-
Agou, T.1
Sekine, M.2
Kawashima, T.3
-
55
-
-
77950458861
-
-
C. H. Lee M. J. Kim S.-P. Han Y.-S. Lee S. K. Kang J. H. Song J. T. Je H.-Y. Oh Y.-J. Kim Tetrahedron 2010 66 3360 3364
-
(2010)
Tetrahedron
, vol.66
, pp. 3360-3364
-
-
Lee, C.H.1
Kim, M.J.2
Han, S.-P.3
Lee, Y.-S.4
Kang, S.K.5
Song, J.H.6
Je, J.T.7
Oh, H.-Y.8
Kim, Y.-J.9
-
57
-
-
45549113785
-
-
A. R. Katritzky C. H. Marson G. Palenik A. E. Koziol H. Luce M. Karelson B.-C. Chen W. Brey Tetrahedron 1988 44 3209 3214
-
(1988)
Tetrahedron
, vol.44
, pp. 3209-3214
-
-
Katritzky, A.R.1
Marson, C.H.2
Palenik, G.3
Koziol, A.E.4
Luce, H.5
Karelson, M.6
Chen, B.-C.7
Brey, W.8
-
59
-
-
78651482571
-
-
This interpretation is in line with preliminary computational results, clearly indicating a substantial barrier for 2-methylnaphthyl rotation in 2b, which drops significantly in the corresponding B-F adduct
-
K. Nikitin H. Müller-Bunz Y. Ortin J. Muldoon M. J. McGlinchey Org. Lett. 2011 13 256 259
-
(2011)
Org. Lett.
, vol.13
, pp. 256-259
-
-
Nikitin, K.1
Müller-Bunz, H.2
Ortin, Y.3
Muldoon, J.4
McGlinchey, M.J.5
-
60
-
-
84883886477
-
-
2O at various pH and to systematically examine the resulting effect on the equilibration rate
-
E. M. L. Fink, Bachelor thesis, Goethe Universität Frankfurt, Frankfurt (Main), Germany, 2010
-
(2010)
Bachelor Thesis
, vol.2
-
-
Fink, E.M.L.1
-
69
-
-
79952130294
-
-
Gaussian, Inc., Wallingford, CT, USA, For an overview, see
-
M. J. Frisch, et al., Gaussian 09, Revision C.01, Gaussian, Inc., Wallingford, CT, USA, 2010
-
(2010)
Gaussian 09, Revision C.01
-
-
Frisch, M.J.1
-
71
-
-
77958048834
-
-
ed., Weinheim, Germany
-
The Quantum Theory of Atoms in Molecules, ed., C. F. Matta, and, R. J. Boyd, Weinheim, Germany, 2007
-
(2007)
The Quantum Theory of Atoms in Molecules
-
-
Matta, C.F.1
Boyd, R.J.2
-
74
-
-
11744305193
-
-
The gas-phase calculations for the dianionic species are of approximate value only: due to the lack of diffuse functions (and the lack of solvation) the electrons in the free dianionic species are formally unbound (the orbital energies are positive)
-
K. Wolinski J. F. Hinton P. Pulay J. Am. Chem. Soc. 1990 112 8251 8260
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 8251-8260
-
-
Wolinski, K.1
Hinton, J.F.2
Pulay, P.3
-
80
-
-
84985633250
-
-
B. Bogdanović N. Janke C. Krüger R. Mynott K. Schlichte U. Westeppe Angew. Chem., Int. Ed. Engl. 1985 24 960 961
-
(1985)
Angew. Chem., Int. Ed. Engl.
, vol.24
, pp. 960-961
-
-
Bogdanović, B.1
Janke, N.2
Krüger, C.3
Mynott, R.4
Schlichte, K.5
Westeppe, U.6
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