-
3
-
-
0032499644
-
-
L. Utschig, Y. Ohigashi, M. Thurnauer, D. Tiede, Biochemistry 1998, 37, 8278-8281
-
(1998)
Biochemistry
, vol.37
, pp. 8278-8281
-
-
Utschig, L.1
Ohigashi, Y.2
Thurnauer, M.3
Tiede, D.4
-
4
-
-
0033023083
-
-
M. Paddock, M. Graige, G. Feher, M. Okamura, Proc. Natl. Acad. Sci. USA 1999, 96, 6183-6188
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 6183-6188
-
-
Paddock, M.1
Graige, M.2
Feher, G.3
Okamura, M.4
-
5
-
-
0034652299
-
-
M. Paddock, G. Feher, M. Okamura, Proc. Natl. Acad. Sci. USA 2000, 97, 1548-1553
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 1548-1553
-
-
Paddock, M.1
Feher, G.2
Okamura, M.3
-
6
-
-
0034696408
-
-
L. Utschig, O. Poluektov, D. Tiede, M. Thurnauer, Biochemistry 2000, 39, 2961-2969
-
(2000)
Biochemistry
, vol.39
, pp. 2961-2969
-
-
Utschig, L.1
Poluektov, O.2
Tiede, D.3
Thurnauer, M.4
-
8
-
-
26444458800
-
-
L. Kálmán, M. Thielges, J. Williams, J. Allen, Biochemistry 2005, 44, 13266-13273.
-
(2005)
Biochemistry
, vol.44
, pp. 13266-13273
-
-
Kálmán, L.1
Thielges, M.2
Williams, J.3
Allen, J.4
-
12
-
-
67650540770
-
-
E. Ohana, E. Hoch, C. Keasar, T. Kambe, O. Yifrach, M. Hershfinkel, I. Sekler, J. Biol. Chem. 2009, 284, 17677-17686.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 17677-17686
-
-
Ohana, E.1
Hoch, E.2
Keasar, C.3
Kambe, T.4
Yifrach, O.5
Hershfinkel, M.6
Sekler, I.7
-
13
-
-
0004240038
-
-
(Ed.: B.L. Feringa), Wiley-VCH, Weinheim
-
Molecular Switches (Ed.:, B.L. Feringa,), Wiley-VCH, Weinheim, 2001
-
(2001)
Molecular Switches
-
-
-
14
-
-
33846152351
-
-
E. R. Kay, D. A. Leigh, F. Zerbetto, Angew. Chem. 2007, 119, 72-196
-
(2007)
Angew. Chem.
, vol.119
, pp. 72-196
-
-
Kay, E.R.1
Leigh, D.A.2
Zerbetto, F.3
-
16
-
-
84890576380
-
-
Wiley-VCH, Weinheim
-
V. Balzani, A. Credi, M. Venturi, Molecular Devices and Machinesa-Concepts and Perspectives for the Nanoworld, Wiley-VCH, Weinheim, 2008
-
(2008)
Molecular Devices and Machinesa-Concepts and Perspectives for the Nanoworld
-
-
Balzani, V.1
Credi, A.2
Venturi, M.3
-
18
-
-
76249131765
-
-
M. vonDelius, E. M. Geertsema, D. A. Leigh, Nat. Chem. 2010, 2, 96-101
-
(2010)
Nat. Chem.
, vol.2
, pp. 96-101
-
-
Vondelius, M.1
Geertsema, E.M.2
Leigh, D.A.3
-
19
-
-
77953889686
-
-
J. Leblond, H. Gao, A. Petitjean, J. Leroux, J. Am. Chem. Soc. 2010, 132, 8544-8545
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8544-8545
-
-
Leblond, J.1
Gao, H.2
Petitjean, A.3
Leroux, J.4
-
20
-
-
77956631756
-
-
Y. Zhao, Z. Li, S. Kabehie, Y. Y. Botros, J. F. Stoddart, J. I. Zink, J. Am. Chem. Soc. 2010, 132, 13016-13025.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 13016-13025
-
-
Zhao, Y.1
Li, Z.2
Kabehie, S.3
Botros, Y.Y.4
Stoddart, J.F.5
Zink, J.I.6
-
21
-
-
79951795911
-
-
For examples of electro- and photochemically induced pH modulations, see
-
For examples of electro- and photochemically induced pH modulations, see
-
-
-
-
22
-
-
69249090640
-
-
V. Balzani, A. Credi, M. Venturi, Chem. Soc. Rev. 2009, 38, 1542-1550
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 1542-1550
-
-
Balzani, V.1
Credi, A.2
Venturi, M.3
-
23
-
-
58449135974
-
-
S. Silvi, E. C. Constable, C. E. Housecroft, J. E. Beves, E. L. Dunphy, M. Tomasulo, F. M. Raymo, A. Credi, Chem. Eur. J. 2009, 15, 178-185
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 178-185
-
-
Silvi, S.1
Constable, E.C.2
Housecroft, C.E.3
Beves, J.E.4
Dunphy, E.L.5
Tomasulo, M.6
Raymo, F.M.7
Credi, A.8
-
24
-
-
77249140006
-
-
M. Frasconi, R. Tel-Vered, J. Elbaz, I. Willner, J. Am. Chem. Soc. 2010, 132, 2029-2036.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 2029-2036
-
-
Frasconi, M.1
Tel-Vered, R.2
Elbaz, J.3
Willner, I.4
-
28
-
-
34548218261
-
-
L. Latheef, E. Manoj, M. R. P. Kurup, Polyhedron 2007, 26, 4107-4113.
-
(2007)
Polyhedron
, vol.26
, pp. 4107-4113
-
-
Latheef, L.1
Manoj, E.2
Kurup, M.R.P.3
-
30
-
-
76149085486
-
-
A. E. Hargrove, Z. Zhong, J. L. Sessler, E. V. Anslyn, New J. Chem. 2010, 34, 348-354.
-
(2010)
New J. Chem.
, vol.34
, pp. 348-354
-
-
Hargrove, A.E.1
Zhong, Z.2
Sessler, J.L.3
Anslyn, E.V.4
-
31
-
-
77951969448
-
-
A.-M. Stadler, J. Ramírez, J. Lehn, Chem. Eur. J. 2010, 16, 5369-5378.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 5369-5378
-
-
Stadler, A.-M.1
Ramírez, J.2
Lehn, J.3
-
32
-
-
79951778874
-
-
2+, see FigureS10
-
2+, see FigureS10.
-
-
-
-
33
-
-
79951803641
-
-
avalue of this system
-
avalue of this system.
-
-
-
-
34
-
-
79951775944
-
-
note
-
2) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
-
-
-
35
-
-
79951776826
-
-
In the crystal structure of Zn(QPH-Z), the dihedral angle between the pyridyl ring and the quinolinyl ring is 12.740(63)°, and the torsion angles of N-N-C-C (pyridyl) and C-N-N-C (quinolinyl) are 178.801(232) and 178.875(235)°, respectively
-
In the crystal structure of Zn(QPH-Z), the dihedral angle between the pyridyl ring and the quinolinyl ring is 12.740(63)°, and the torsion angles of N-N-C-C (pyridyl) and C-N-N-C (quinolinyl) are 178.801(232) and 178.875(235)°, respectively.
-
-
-
-
36
-
-
79951780439
-
-
note
-
2) value was 0.2125 (all data).
-
-
-
-
37
-
-
79951788279
-
-
Hydrogen atom H7 of one ligand is oriented perpendicularly to the deprotonated hydrazone functional group of the other; hence, it is shielded
-
Hydrogen atom H7 of one ligand is oriented perpendicularly to the deprotonated hydrazone functional group of the other; hence, it is shielded.
-
-
-
-
38
-
-
79951791688
-
-
2+. We see no evidence of this coordination, thus further supporting the intramolecular pathway. This said, we cannot absolutely rule out intermolecular proton transfer
-
2+. We see no evidence of this coordination, thus further supporting the intramolecular pathway. This said, we cannot absolutely rule out intermolecular proton transfer.
-
-
-
-
39
-
-
79951777363
-
-
M. J. Wiester, P. A. Ulmann, C. A. Mirkin, Angew. Chem. 2011, 123, 118-142
-
(2011)
Angew. Chem.
, vol.123
, pp. 118-142
-
-
Wiester, M.J.1
Ulmann, P.A.2
Mirkin, C.A.3
|