-
6
-
-
0043235469
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-
For the monooxygenases, the copper ion is coordinated to two histidines and one methionine (see [4])
-
For the monooxygenases, the copper ion is coordinated to two histidines and one methionine (see [4]).
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-
-
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7
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0033583557
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Chaudhuri P., Hess M., Weyhermüller T., Wieghardt K., Angew. Chem. Int. Edit. 38 (1999) 1095.
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(1999)
Angew. Chem. Int. Edit.
, vol.38
, pp. 1095
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-
Chaudhuri, P.1
Hess, M.2
Weyhermüller, T.3
Wieghardt, K.4
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16
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0038633748
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Sénèque O., Rager M.-N., Giorgi M., Reinaud O., J. Am. Chem. Soc. 122 (2000) 61083.
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 61083
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-
Sénèque, O.1
Rager, M.-N.2
Giorgi, M.3
Reinaud, O.4
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17
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0032538471
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Blanchard S., Le Clainche L., Rager M.-N., Chansou B., Tuchagues J.-P., Duprat A.F., Mest Y.L., Reinaud O. Angew. Chem. Int. Edit. 37:1998;2732.
-
(1998)
Angew. Chem. Int. Edit.
, vol.37
, pp. 2732
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-
Blanchard, S.1
Le Clainche, L.2
Rager, M.-N.3
Chansou, B.4
Tuchagues, J.-P.5
Duprat, A.F.6
Mest, Y.L.7
Reinaud, O.8
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19
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0034680518
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Rondelez Y., Sénèque O., Rager M.-N., Duprat A., Reinaud O., Chem. Eur. J. 6 (2000) 4218.
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(2000)
Chem. Eur. J.
, vol.6
, pp. 4218
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-
Rondelez, Y.1
Sénèque, O.2
Rager, M.-N.3
Duprat, A.4
Reinaud, O.5
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21
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0042233260
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The calixarenes were sketched and optimized by using the esff force field of the Biosym package Insight/Discover (Release 95.0, Biosym/MSI, San Diego, CA, 1995), on an IBM RISC 6K workstation. The standard Discover 3 algorithms were selected with their default inputs (0.001 for BFGS Newton energy convergence). Due to the medium size of the molecules, no cutoff was used to compute the non-bond contribution
-
The calixarenes were sketched and optimized by using the esff force field of the Biosym package Insight/Discover (Release 95.0, Biosym/MSI, San Diego, CA, 1995), on an IBM RISC 6K workstation. The standard Discover 3 algorithms were selected with their default inputs (0.001 for BFGS Newton energy convergence). Due to the medium size of the molecules, no cutoff was used to compute the non-bond contribution.
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-
-
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22
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0043235444
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The spectroscopic studies indicate that these geometrical changes are not related to the nature of the N-alkyl group nor that of the counter anion
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The spectroscopic studies indicate that these geometrical changes are not related to the nature of the N-alkyl group nor that of the counter anion.
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-
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23
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37049096497
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Addison A.W., Rao T.N., Reedijk J., van Rijn J., Verschoor G.C., J. Chem. Soc., Dalton Trans. (1984) 1349.
-
(1984)
J. Chem. Soc., Dalton Trans.
, pp. 1349
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-
Addison, A.W.1
Rao, T.N.2
Reedijk, J.3
Van Rijn, J.4
Verschoor, G.C.5
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24
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0042233263
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This has been studied in details with the zinc complexes (see ref. [16])
-
This has been studied in details with the zinc complexes (see ref. [16]).
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-
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25
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0032508920
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2+ is not and may be related to the electronic structure of the complex. Curiously also, no d-d transition was observed (at least below 1 000 nm) for the phenol adduct which was EPR silent at 120 K. Its EPR signal was observable only below 30 K. Such a behaviour is very unsusual. For a previous related example, see
-
2+ is not and may be related to the electronic structure of the complex. Curiously also, no d-d transition was observed (at least below 1 000 nm) for the phenol adduct which was EPR silent at 120 K. Its EPR signal was observable only below 30 K. Such a behaviour is very unsusual. For a previous related example, see: Schneider J.L., Carrier S.M., Ruggiero C.E., Young V.G.J., Tolman W.B., J. Am. Chem. Soc. 120 (1998) 11408.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 11408
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-
Schneider, J.L.1
Carrier, S.M.2
Ruggiero, C.E.3
Young, V.G.J.4
Tolman, W.B.5
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26
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0042233261
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We are currently working on the identification of the oxidation products
-
We are currently working on the identification of the oxidation products.
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-
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27
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0043235441
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In the case of the other phenol derivatives, a very fast decrease to 0 of the electrolytic current indicates a passivation of the electrode. This might be the result of a polymerisation on the electrode either by catalytic oxidation or by direct oxidation of these phenols. Their oxidation potential are lower than that of the pFPhOH
-
In the case of the other phenol derivatives, a very fast decrease to 0 of the electrolytic current indicates a passivation of the electrode. This might be the result of a polymerisation on the electrode either by catalytic oxidation or by direct oxidation of these phenols. Their oxidation potential are lower than that of the pFPhOH.
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28
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0031900123
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Wada A., Harata M., Hasegawa K., Jitsukawa K., Masuda H., Mukai M., Kitagawa T., Einaga H. Angew. Chem. Int. Edit. 37:1998;798.
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(1998)
Angew. Chem. Int. Edit.
, vol.37
, pp. 798
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Wada, A.1
Harata, M.2
Hasegawa, K.3
Jitsukawa, K.4
Masuda, H.5
Mukai, M.6
Kitagawa, T.7
Einaga, H.8
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29
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0003666167
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University of Glasgow, Scotland, UK, Nonius BV, Delft, The Netherlands and MacScience Co. Ltd., Yokohama, Japan
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Mackay S., Gilmore C.J., Edwards C., Tremayne M., Stewart N., Shackland K., maXus: a computer program for the solution and refinement of crystal structures from diffraction data, University of Glasgow, Scotland, UK, Nonius BV, Delft, The Netherlands and MacScience Co. Ltd., Yokohama, Japan, 1998.
-
(1998)
Maxus: A Computer Program for the Solution and Refinement of Crystal Structures from Diffraction Data
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Mackay, S.1
Gilmore, C.J.2
Edwards, C.3
Tremayne, M.4
Stewart, N.5
Shackland, K.6
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