Academic Journal

Ligation of Boratabenzene and 9‑Borataphenanthrene to Coinage Metals

التفاصيل البيبلوغرافية
العنوان: Ligation of Boratabenzene and 9‑Borataphenanthrene to Coinage Metals
المؤلفون: Greta K. Wisofsky (11814151), Katherine Rojales (11814154), Xiaojun Su (223221), Tyler A. Bartholome (10223646), Andrew Molino (5463602), Aishvaryadeep Kaur (4047199), David J. D. Wilson (7537427), Jason L. Dutton (1527514), Caleb D. Martin (1446844)
سنة النشر: 2021
المجموعة: Smithsonian Institution: Digital Repository
مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Molecular Biology, Pharmacology, Cancer, Computational Biology, Chemical Sciences not elsewhere classified, heterocyclic carbene switched, group 11 ph, carbon atom much, vacating coordination sites, 9 ‑ borataphenanthrene, 6 , 2 , 3 , copper boratabenzene species, coordination complexes, borataphenanthrene anions, metal center, coinage metals, borataalkene unit, ancillary ligand
الوصف: The reactions of boratabenzene and borataphenanthrene anions with group 11 Ph 3 PMCl reagents furnished η 2 coordination complexes, with the exception of the copper boratabenzene species that adopted an η 6 mode. The binding of arene ligands to copper in an η 6 manner is rare, and altering the ancillary ligand on copper to an N-heterocyclic carbene switched the binding of the boratabenzene to η 2 , indicating that such ligands are capable of vacating coordination sites. The η 2 coordination complexes bind side-on, akin to olefins, via a borataalkene unit, although with the carbon atom much more proximal to the metal center than boron.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
Relation: https://figshare.com/articles/journal_contribution/Ligation_of_Boratabenzene_and_9_Borataphenanthrene_to_Coinage_Metals/17148280
DOI: 10.1021/acs.inorgchem.1c02800.s001
الاتاحة: https://doi.org/10.1021/acs.inorgchem.1c02800.s001
Rights: CC BY-NC 4.0
رقم الانضمام: edsbas.5982BF24
قاعدة البيانات: BASE
الوصف
DOI:10.1021/acs.inorgchem.1c02800.s001