127. Ferrocene derivatives. Part V. Ferrocenealdehyde

Broadhead, Geoffrey D.; Osgerby, J. M.; Pauson, P. L.

doi:10.1039/jr9580000650

Cited by 131 publications

(62 citation statements)

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“…Cyanoferrocene was prepared from ferrocenecarboxaldehyde via ferrocenecarboxaldoxime (Broadhead, Osgerby & Pauson, 1958). Crystals suitable for single-crystal diffraction were grown from cyclohexane solution.…”

Section: Methodsmentioning

confidence: 99%

Cyanoferrocene: a Two-Dimensional Network Generated by Short C—H.N Hydrogen Bonds

Bell¹,

Ferguson²,

Glidewell³

1996

Acta Crystallogr C

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Section: Methodsmentioning

confidence: 99%

Cyanoferrocene: a Two-Dimensional Network Generated by Short C—H.N Hydrogen Bonds

Bell¹,

Ferguson²,

Glidewell³

1996

Acta Crystallogr C

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“…Solvents were purified according to conventional procedures and were freshly distilled prior to use. Compounds 4 [14,15], 5 [16,17], 8 [13,18], ferrocenylnitrile [19], ferrocenylacetylene [20,21] and AIH 3 ' NMe3 [22] were prepared as described in the literature. IR spectra were recorded on a Bio-Rad Digilab FTS7 spectrometer.…”

Section: Materials and Equipmentmentioning

confidence: 99%

Synthesis and electrochemical behavior of the ferrocenyl units assembled on imidoalane and carbaalane clusters

Kumar

Roesky

Andronesi

et al. 2005

Inorganica Chimica Acta

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Hydroalumination reaction was effectively carried out on ferrocenylnitrile in the synthesis of imidoalane cluster [HAl NCH 2 C 5 H 4FeCp]6 (3). Compound 3 exhibits a reversible electrochemical behavior. In the presence of ferrocenylmethanol, meta thesis reactions were carried out on [HAlNCH 2 (C 4 H)S)]6 (4) and [HAlNCH 2 Ph]6 (5) in the synthesis of [CpFeC s H4 CH 2 0AlNCH2CC 4 H)S)]6 (6) and [CpFeC s H 4 CH 2 0AlNCH 2 Ph]6 (7). The ferrocenylmethoxide groups present in these two com pounds show a single reversible oxidation wave, which suggests their electrochemical equivalence. Electrochemical studies were also carried out on the carbaalane [(AIHhCFcC CAlMAlNMe3hCCCH2Ph)6] (9), which exhibited a considerably broadened wave with shoulders preceding the main anodic and cathodic peak, and it can be assigned to weak electronic interactions between the individ ual ferrocenyl sites.

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“…1, 142.3, 139.1, 137.8, 135.4, 130.0, 129.2, 129.1, 128.8, 128.2, 124.1, 122.3, 63.0 11;H,4.84;N,6.11. Found: C,68.34;H,4.72;N,6.27. …”

mentioning

confidence: 99%

Synthesis of Substituted Biarylmethanol via Ferrocenyloxime Palladacycles Catalyzed Suzuki Reaction of Chlorophenylmethanol in Water

Li¹,

Feng²,

Liu³

2014

Bulletin of the Korean Chemical Society

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127. Ferrocene derivatives. Part V. Ferrocenealdehyde

Cited by 131 publications

References 0 publications

Cyanoferrocene: a Two-Dimensional Network Generated by Short C—H.N Hydrogen Bonds

Cyanoferrocene: a Two-Dimensional Network Generated by Short C—H.N Hydrogen Bonds

Synthesis and electrochemical behavior of the ferrocenyl units assembled on imidoalane and carbaalane clusters

Synthesis of Substituted Biarylmethanol via Ferrocenyloxime Palladacycles Catalyzed Suzuki Reaction of Chlorophenylmethanol in Water

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