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Cyclobutadiene (and Its Higher Homologues) Complexes of the s-, p-, d-, and f-Block Elements Full article

Journal Organometallics
ISSN: 1520-6041 , E-ISSN: 0276-7333
Output data Year: 2026, Volume: 45, DOI: 10.1021/acs.organomet.6c00214
Authors Lee Vladimir Ya. 1,2,3,4 , Ananikov Valentine P. 2 , Egorov Mikhail P. 2 , Syroeshkin Mikhail A. 2
Affiliations
1 Shenzhen MSU−BIT University
2 N. D. Zelinsky Institute of Organic Chemistry RAS
3 Saitama University
4 University of Tsukuba

Abstract: Square-planar triplet cyclobutadiene is intrinsically unstable, given its four π-electron configuration leading to unavoidable antiaromatic destabilization. One effective way to stabilize cyclobutadiene is through its incorporation into the coordination sphere of an element capable of electron donation. Metals (main group metals, transition metals, lanthanides, and actinides) are most frequently used as electron-donating elements, although recently, it was established that the main group elements may also serve as capping donors in cyclobutadiene complexes. The recent advances in the chemistry of the cyclobutadiene complexes of the s-, p-, d-, and f-block elements are briefly summarized in this review.
Cite: Lee V.Y. , Ananikov V.P. , Egorov M.P. , Syroeshkin M.A.
Cyclobutadiene (and Its Higher Homologues) Complexes of the s-, p-, d-, and f-Block Elements
Organometallics. 2026. V.45. DOI: 10.1021/acs.organomet.6c00214 WOS OpenAlex
Dates:
Submitted: Jun 16, 2026
Accepted: Sep 15, 2026
Published online: Oct 8, 2026
Identifiers:
≡ Web of science: WOS:001897874000001
≡ OpenAlex: W7220907714
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