Ferrole

Structure of the ferrole Fe2C4H4(CO)6.[1] Color scheme: red = O, gray = C, dark blue = Fe, white = H.

Not to be confused with Ferrule.

In organoiron chemistry, a ferrole is a type of diiron complex containing the (OC)3FeC4R4 heterocycle that is pi-bonded to a Fe(CO)3 group. These compounds have Fe-Fe bonds (ca. 252 pm) and semi-bridging CO ligands (Fe-C distances = 178, 251 pm). They are typically air-stable, soluble in nonpolar solvents, and red-orange in color.[2]

## Synthesis

Ferroles typically arise by the reaction of alkynes with iron carbonyls. Such reactions are known to generate many products, e.g. complexes of cyclopentadienones and para-quinones.[3][4]

Another route involves the desulfurization of thiophenes (SC4R4) by iron carbonyls, shown in the following idealized equation:

Fe3(CO)12 \+ SC4R4 → Fe2(CO)6C4R4 \+ FeS + 6 CO

An unusual route to ferroles involves treatment of Collman's reagent with trimethylsilyl chloride (tms = (CH3)3Si):

2 Na2Fe(CO)4 \+ 4 tmsCl → Fe2(CO)6C4(Otms)4 \+ 2 CO + 4 NaCl

## Reactions

Some ferroles react with tertiary phosphines to give the substituted flyover complex Fe2(CO)5(PR3)(C4R4CO).[5] [6]

## References

1. ↑ Dettlaf, Gerd; Weiss, Erwin (1976). "Kristallstruktur, 1H-NMR- und Massenspektrum von Tricarbonylferracyclopentadien-tricarbonyleisen, C4H4Fe2(CO)6". Journal of Organometallic Chemistry 108 (2): 213–223. doi:10.1016/S0022-328X(00)82143-9.
2. ↑ Fehlhammer, W.P.; Stolzenberg, H. (1982). "Dinuclear Iron Compounds with Hydrocarbon Ligands". Comprehensive Organometallic Chemistry. pp. 513–613. doi:10.1016/B978-008046518-0.00051-9. ISBN 9780080465180.
3. ↑ Organic Syntheses via Metal Carbonyls Volume 1. NY: Wiley Interscience. 1968.
4. ↑ Bird, C. W. (1962). "Synthesis of Organic Compounds by Direct Carbonylation Reactions Using Metal Carbonyls". Chemical Reviews 62 (4): 283–302. doi:10.1021/cr60218a001.
5. ↑ Giordano, Roberto; Sappa, Enrico; Cauzzi, Daniele; Predieri, Giovanni; Tiripicchio, Antonio (1996). "Reactions of the 'ferrole' complex [Fe2(CO)6(C2Et2)2] with group 15 donor ligands and with alkynes. Stepwise formation and disengagement of tropones. Crystal and molecular structure of [Fe2(CO)5{(CEt)2 CO(CEt)2 CHCPH}]". Journal of Organometallic Chemistry 511 (1–2): 263–271. doi:10.1016/0022-328X(95)05936-J.
6. ↑ Fagan, Paul J. (1995). "Dinuclear Iron Compounds with Hydrocarbon Ligands". Comprehensive Organometallic Chemistry II. pp. 231–258. doi:10.1016/B978-008046519-7.00058-7. ISBN 9780080465197.

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Ferrole. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Ferrole&oldid=1059456"