24:
207:
Knölker, Hans-Joachim; Baum, Elke; Goesmann, Helmut; Klauss, Rüdiger (1999). "Demetalation of
Tricarbonyl(cyclopentadienone)iron Complexes Initiated by a Ligand Exchange Reaction with NaOH—X-Ray Analysis of a Complex with Nearly Square-Planar Coordinated Sodium".
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H centre. It is generated by the corresponding cyclopentadienone tricarbonyl by treatment with base followed by acidification. The compound is related to the
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Casey, Charles P.; Guan, Hairong (2007). "An
Efficient and Chemoselective Iron Catalyst for the Hydrogenation of Ketones".
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10.1002/(SICI)1521-3773(19990712)38:13/14<2064::AID-ANIE2064>3.0.CO;2-W
151:, a hydroxycyclopentadienyl derivative that also functions as a catalyst for
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104:
Except where otherwise noted, data are given for materials in their
245:"An Iron Catalyst for Ketone Hydrogenations under Mild Conditions"
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8:
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260:
174:Journal of the American Chemical Society
249:Angewandte Chemie International Edition
210:Angewandte Chemie International Edition
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7:
14:
135:. The complex features an hydroxy
22:
108:(at 25 °C , 100 kPa).
1:
243:Bullock, R. Morris (2007).
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316:Cyclopentadienyl complexes
131:, which is a catalyst for
139:ligand bound to an Fe(CO)
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57:
30:
21:
306:Trimethylsilyl compounds
145:organoruthenium compound
321:Half sandwich compounds
301:Hydrogenation catalysts
98:polar organic solvents
262:10.1002/anie.200703053
133:transfer hydrogenation
291:Organoiron compounds
216:(13–14): 2064–2066.
129:organoiron compound
93:Solubility in water
18:
326:Iron(II) compounds
296:Carbonyl complexes
112:Infobox references
16:
255:(39): 7360–7363.
186:10.1021/ja071159f
180:(18): 5816–5817.
120:Chemical compound
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137:cyclopentadienyl
65:Chemical formula
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26:
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17:Knölker complex
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125:Knölker complex
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311:Metal hydrides
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149:Shvo's complex
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106:standard state
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153:hydrogenation
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31:Identifiers
58:Properties
48:243866-64-0
285:Categories
159:References
38:CAS Number
271:17847139
230:34182704
194:17439131
147:called
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127:is an
267:PMID
226:PMID
190:PMID
123:The
257:doi
218:doi
182:doi
178:129
78:FeO
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253:46
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214:38
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82:Si
76:28
72:17
273:.
259::
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220::
196:.
184::
141:2
84:2
80:3
74:H
70:C
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