-
2
-
-
12944325649
-
-
Chapter 33. Academic Press: Kadish, K. M., Smith, K. M., Guilard, R., Eds.; New York, in press. Personal communication from G. B. Richter-Addo
-
(b) Cheng, L.; Richter-Addo, G. B. Chapter 33. In The Prophyrin Handbook; Academic Press: Kadish, K. M., Smith, K. M., Guilard, R., Eds.; New York, in press. Personal communication from G. B. Richter-Addo.
-
The Prophyrin Handbook
-
-
Cheng, L.1
Richter-Addo, G.B.2
-
5
-
-
0002603415
-
-
Ellison, M. K.; Schulz, C. E.; Scheidt, W. R. Inorg. Chem. 1999, 38, 100-108.
-
(1999)
Inorg. Chem.
, vol.38
, pp. 100-108
-
-
Ellison, M.K.1
Schulz, C.E.2
Scheidt, W.R.3
-
8
-
-
0032544948
-
-
(c) Lorkovic, I. M.; Miranda, K. M.; Lee, B. L.; Bernhard, S.; Schoonover, J. M.; Ford, P. C. J. Am. Chem. Soc. 1998, 120, 11674-11683.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 11674-11683
-
-
Lorkovic, I.M.1
Miranda, K.M.2
Lee, B.L.3
Bernhard, S.4
Schoonover, J.M.5
Ford, P.C.6
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10
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12944308674
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note
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3. Warning: at -78°C, considerable NO absorbs in the column and precaution should be taken for the controlled NO release when the system warms to room temperature. Solutions were prepared and transferred to cells with gastight syringes inside an inert atmosphere "drybox". Materials in contact with NO solutions (septa, stopcocks, and plungers) were deaerated by storage in the drybox for at least 18 h prior to solution exposure.
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11
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12944303991
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note
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8b who presented evidence that low-T toluene solutions of 1 under NO demonstrate reversible changes in the EPR and optical spectra consistent with the formation of the dinitrosyl. NMR experiments in this laboratory are in agreement with the observation that such a species may be formed at low temperature but not at ambient temperature. It is also notable that there were no indications in Wayland's spectra that 1 reacts further with NO to give 2 at room or lower T.
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13
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0000510919
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(a) Kadish, K. M.; Adamian, V. A.; Van Caemelbecke, E.; Tan, Z.; Tagliatesta, P.; Bianco, P.; Boschi, T.; Yi, G.-B.; Khan, M. A.; Richter-Addo, G. B. Inorg. Chem. 1996, 35, 1343-1348.
-
(1996)
Inorg. Chem.
, vol.35
, pp. 1343-1348
-
-
Kadish, K.M.1
Adamian, V.A.2
Van Caemelbecke, E.3
Tan, Z.4
Tagliatesta, P.5
Bianco, P.6
Boschi, T.7
Yi, G.-B.8
Khan, M.A.9
Richter-Addo, G.B.10
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14
-
-
0001240364
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-
(b) Miranda, K. M.; Bu, X.; Lorkovic, I. M.; Ford, P. C. Inorg. Chem. 1997, 36, 4838-4848.
-
(1997)
Inorg. Chem.
, vol.36
, pp. 4838-4848
-
-
Miranda, K.M.1
Bu, X.2
Lorkovic, I.M.3
Ford, P.C.4
-
16
-
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0027253654
-
-
(b) Ford, P. C.; Wink, D. A.; Stanbury, D. M. FEBS Lett. 1993, 326, 1-3.
-
(1993)
FEBS Lett.
, vol.326
, pp. 1-3
-
-
Ford, P.C.1
Wink, D.A.2
Stanbury, D.M.3
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18
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0000399717
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-
(a) Hoshino, M.; Ozawa, K.; Seki, H.; Ford, P. C. J. Am. Chem. Soc. 1993, 115, 9568-9575.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9568-9575
-
-
Hoshino, M.1
Ozawa, K.2
Seki, H.3
Ford, P.C.4
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19
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12944299646
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note
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3 must have a larger value in the former.
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22
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0001364915
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(a) Frangione, M.; Port, J.; Baldiwala, M.; Judd, A.; Galley, J.; DeVega, M.; Linna, K.; Caron, L.; Anderson, E.; Goodwin, J. A. Inorg. Chem. 1997, 36, 1904-1911.
-
(1997)
Inorg. Chem.
, vol.36
, pp. 1904-1911
-
-
Frangione, M.1
Port, J.2
Baldiwala, M.3
Judd, A.4
Galley, J.5
DeVega, M.6
Linna, K.7
Caron, L.8
Anderson, E.9
Goodwin, J.A.10
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24
-
-
0000892965
-
-
(c) Phillippi, M. A.; Baenziger, N.; Goff, H. M. Inorg. Chem. 1981, 20, 3904-3911.
-
(1981)
Inorg. Chem.
, vol.20
, pp. 3904-3911
-
-
Phillippi, M.A.1
Baenziger, N.2
Goff, H.M.3
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25
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12944325152
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note
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2O may interact with 1 to inhibit its reactivity with NO. However, solutions of 1 plus NO prepared in an oven-dried silanized UV/vis cell by vacuum line transfer of toluene from highly activated 3 Å molecular sieves (to minimize such traces) demonstrated no differences in reactivity.
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26
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12944321216
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Personal communication
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(b) Farmer, P. J. Personal communication.
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Farmer, P.J.1
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