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P. R. Ortiz de Montellano, Ed. Plenum Press, New York, ed. 2, and references therein
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J. T. Groves and Y.-Z. Han, in Cytochrome P-450, Structure, Mechanism and Biochemistry, P. R. Ortiz de Montellano, Ed. (Plenum Press, New York, ed. 2, 1995), pp. 3-48 and references therein; M. Réglier, C. Jorand, B. Waegell, J. Chem. Soc. Chem. Commun. 1990, 1752 (1990); W. O. Koch and H. J. Krüger, Angew. Chem. Int. Ed. Engl. 34, 2671 (1996).
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Groves, J.T.1
Han, Y.-Z.2
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J. T. Groves and Y.-Z. Han, in Cytochrome P-450, Structure, Mechanism and Biochemistry, P. R. Ortiz de Montellano, Ed. (Plenum Press, New York, ed. 2, 1995), pp. 3-48 and references therein; M. Réglier, C. Jorand, B. Waegell, J. Chem. Soc. Chem. Commun. 1990, 1752 (1990); W. O. Koch and H. J. Krüger, Angew. Chem. Int. Ed. Engl. 34, 2671 (1996).
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Réglier, M.1
Jorand, C.2
Waegell, B.3
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3
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33748238499
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J. T. Groves and Y.-Z. Han, in Cytochrome P-450, Structure, Mechanism and Biochemistry, P. R. Ortiz de Montellano, Ed. (Plenum Press, New York, ed. 2, 1995), pp. 3-48 and references therein; M. Réglier, C. Jorand, B. Waegell, J. Chem. Soc. Chem. Commun. 1990, 1752 (1990); W. O. Koch and H. J. Krüger, Angew. Chem. Int. Ed. Engl. 34, 2671 (1996).
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Angew. Chem. Int. Ed. Engl.
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Koch, W.O.1
Krüger, H.J.2
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6
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0024557102
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M. M. Whittaker, V. L. DeVito, S. A. Asher, J. W. Whittaker, J. Biol. Chem. 264, 7104 (1989).
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Whittaker, M.M.1
DeVito, V.L.2
Asher, S.A.3
Whittaker, J.W.4
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7
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0030460515
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I. E. Markó et al., Science 274, 2044 (1996); C. Zondervan, R. Hage, B. L. Feringa, Chem. Commun. 1997, 419 (1997).
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Science
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Markó, I.E.1
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8
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1542711441
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I. E. Markó et al., Science 274, 2044 (1996); C. Zondervan, R. Hage, B. L. Feringa, Chem. Commun. 1997, 419 (1997).
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Zondervan, C.1
Hage, R.2
Feringa, B.L.3
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9
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0030818539
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and references therein
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For GOase model studies, see J. A. Halfen et al. [J. Am. Chem. Soc. 119, 8217 (1997)] and references therein.
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J. Am. Chem. Soc.
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Halfen, J.A.1
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10
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0026084786
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N. Ito et al., Nature 350, 87 (1991); N. Ito et al., J. Mol. Biol. 238, 794 (1994).
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Nature
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Ito, N.1
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11
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0028290823
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N. Ito et al., Nature 350, 87 (1991); N. Ito et al., J. Mol. Biol. 238, 794 (1994).
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Ito, N.1
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12
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0030476115
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Y. Wang and T. D. P. Stack, J. Am. Chem. Soc. 118, 13097 (1996). These model complexes are shown to catalytically convert benzyl alcohol to benzaldehyde with a strong organic-radical oxidant.
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J. Am. Chem. Soc.
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, pp. 13097
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Wang, Y.1
Stack, T.D.P.2
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13
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14444274661
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-
note
-
w) = 8.7(9.7).
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-
-
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14
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0000744147
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II value for [Cu(II)BDB] is 2.231, whereas that for its square-planar analog (a cyclohexyl-1,2-diimine backbone) is smaller at 2.195 [E. I. Solomon, Comm. Inorg. Chem. III, 227 (1984)].
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(1984)
Comm. Inorg. Chem.
, vol.3
, pp. 227
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Solomon, E.I.1
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15
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14444288849
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The stoichiometry has been determined by both EPR (77 K) and optical titrations (RT)
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The stoichiometry has been determined by both EPR (77 K) and optical titrations (RT).
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-
-
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16
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14444277571
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note
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-].
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-
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18
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0030804536
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J. L. DuBois et al., ibid. 119, 8578 (1997).
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(1997)
Ibid.
, vol.119
, pp. 8578
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DuBois, J.L.1
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20
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0000348938
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-
-1 yielded first coordination shells easily resolvable into two or three average ligand distances per complex. The [Cu (II)BDB] distances agree very well with x-ray cristallographic data for [Cu(II)BSI] (Fig. 1 legend).
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(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 1566
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Westre, T.E.1
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21
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1842365490
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+•, 2.0057; 2,4-dibromophenoxyl, 2.0061. See Fig. 1 legend for nomenclature. Stable Zn phenoxyl-radical species have been reported [A. Sokolowski et al., J. Am. Chem. Soc. 119, 8889 (1997)].
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(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 8889
-
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Sokolowski, A.1
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22
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14444267869
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-
note
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See supporting information (available upon request or through the Science Online Web site at www. sciencemag.org) for synthetic details, spectroscopic data for all new compounds, and x-ray crystal structural information.
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-
-
-
23
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0039246584
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This study concerns the coordination geometry of Ni complexes [G. J. Colpas et al., Inorg. Chem. 30, 920 (1991)].
-
(1991)
Inorg. Chem.
, vol.30
, pp. 920
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Colpas, G.J.1
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26
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0001942278
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Structural characterization of a phenoxyl-radical chromium complex shows only a +0.02 Å increase in the Cr-OPh bond distance relative to the phenoxy ligand [A. Sokolowski et al., J. Chem. Soc. Chem. Commun. 1996, 1671 (1996)].
-
(1996)
J. Chem. Soc. Chem. Commun.
, vol.1996
, pp. 1671
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Sokolowski, A.1
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27
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14444280459
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Both lithium and sodium alkoxides are suitable
-
Both lithium and sodium alkoxides are suitable.
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-
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28
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37049084868
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2 as the oxidant with either a stoichiometric or an excess amount of base, respectively [N. Kitajima, K. Whang, Y. Moro-oka, A. Uchida, Y. Sasada, J. Chem. Soc. Chem. Commun. 1986, 1504 (1986); J. T. Groves and K.-T. Park, in Studies in Organic Chemistry: The Role of Oxygen in Chemistry and Biochemistry, W. Ando and Y. Moro-oka, Eds. (Elsevier, Amsterdam, 1988), vol. 33, pp. 541-548].
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(1986)
J. Chem. Soc. Chem. Commun.
, vol.1986
, pp. 1504
-
-
Kitajima, N.1
Whang, K.2
Moro-oka, Y.3
Uchida, A.4
Sasada, Y.5
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29
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14444280215
-
-
W. Ando and Y. Moro-oka, Eds. Elsevier, Amsterdam
-
2 as the oxidant with either a stoichiometric or an excess amount of base, respectively [N. Kitajima, K. Whang, Y. Moro-oka, A. Uchida, Y. Sasada, J. Chem. Soc. Chem. Commun. 1986, 1504 (1986); J. T. Groves and K.-T. Park, in Studies in Organic Chemistry: The Role of Oxygen in Chemistry and Biochemistry, W. Ando and Y. Moro-oka, Eds. (Elsevier, Amsterdam, 1988), vol. 33, pp. 541-548].
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(1988)
Studies in Organic Chemistry: The Role of Oxygen in Chemistry and Biochemistry
, vol.33
, pp. 541-548
-
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Groves, J.T.1
Park, K.-T.2
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32
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0001727765
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T. E. King, H. S. Mason, M. Morrison, Eds. University Park Press, Baltimore, MD
-
G. A. Hamilton, J. De Jersey, P. K. Adolf, in Oxidases and Related Redox Systems. T. E. King, H. S. Mason, M. Morrison, Eds. (University Park Press, Baltimore, MD, 1973), vol. 1, pp. 103-124.
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(1973)
Oxidases and Related Redox Systems
, vol.1
, pp. 103-124
-
-
Hamilton, G.A.1
De Jersey, J.2
Adolf, P.K.3
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33
-
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14444269531
-
-
note
-
- transfer.
-
-
-
-
34
-
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14444275374
-
-
note
-
2OH will certainly be much higher, the ratio of the values should remain effectively constant.
-
-
-
-
36
-
-
0001074034
-
-
are also observed
-
2 with KI containing starch and an aqueous Ti(IV) reagent [W. C. Wolfe, Anal. Chem. 34, 1328 (1962)] are also observed.
-
(1962)
Anal. Chem.
, vol.34
, pp. 1328
-
-
Wolfe, W.C.1
-
40
-
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14444274186
-
-
note
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+• species. However, these complexes do not oxidize alcohols.
-
-
-
-
41
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14444278138
-
-
note
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Supported by grants from NIH [GM50730 (T.D.P.S.)], NIH [RR-01209 and NSF CHE-9423181 (K.O.H.)], and a Shell Faculty Career Initiation Award (T.D.P.S.). We thank the UCSF Mass Spectrometry Facility. SSRL operations are funded by the Department of Energy (DOE), Office of Basic Energy Sciences. The Biotechnology Program is supported by the NIH, National Center for Research Resources, Biomedical Technology Program. Further support is provided by the DOE, Office of Biological and Environmental Research.
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