Today, Transition metal formyl complex continues to be a topic of great interest and relevance in today's society. Whether due to its impact on people's daily lives, its influence on popular culture or its importance in academia and science, Transition metal formyl complex continues to be the subject of constant analysis and debate. In this article, we will explore different aspects related to Transition metal formyl complex, from its history and evolution to its current state and possible future developments. Through this analysis, we hope to shed light on the importance and relevance of Transition metal formyl complex today and its impact on different aspects of society.
In organometallic chemistry, a transition metal formyl complex is a metal complex containing one (usually) or more formyl (CHO) ligand. A subset of transition metal acyl complexes, formyl complexes can be viewed as metalla-aldehydes. A representative example is (CO)5ReCHO. The formyl is viewed as an X (pseudohalide) ligand. Metal formyls are proposed as intermediates in the hydrogenation of carbon monoxide, as occurs in the Fischer-Tropsch process.[2]
Structure and bonding
The MCHO group is planar. A C=O double bond is indicated by X-ray crystallography. A second resonance structure has a M=C double bond, with negative charge on oxygen.
Synthesis and reactions
Metal formyl complexes are often prepared by the reaction of metal carbonyls with hydride reagents:[3]
+ + H− → (CO)5ReCHO
The CO ligand is the electrophile and the hydride (provided typically from a borohydride) is the nucleophile.
Some metal formyls are produced by reaction of metal carbonyl anions with reagents that donate the equivalent of a formyl cation, such a mixed formate anhydrides.[4]
Metal formyls participate in many reactions, many of which are motivated by interest in Fischer-Tropsch chemistry. O-alkylation gives carbenoid complexes. The formyl ligand also functions as a base, allowing the formation of M-CH=O-M' linkages.[5] Decarbonylation leads to de-insertion of the carbonyl, yielding hydride complexes.[2]
References
^Wong, Wai-Kwok; Tam, Wilson; Strouse, C. E.; Gladysz, J. A. (1979). "X-Ray crystal structure and chemical transformations of the neutral metal formyl [(η-C5H5)Re(PPh3)(NO)(CHO)]". J. Chem. Soc., Chem. Commun. (12): 530–532. doi:10.1039/C39790000530.
^Maity, Ayan; Teets, Thomas S. (2016). "Main Group Lewis Acid-Mediated Transformations of Transition-Metal Hydride Complexes". Chemical Reviews. 116 (15): 8873–8911. doi:10.1021/acs.chemrev.6b00034. PMID27164024.
^Collman, J. P.; Winter, S. R. (1973). "Isolation and Characterization of a Kinetically Stable transition Metal Formyl complex". Journal of the American Chemical Society. 95 (12): 4089–4090. doi:10.1021/ja00793a066.