@article {49602,
	title = {Pair of dinuclear Fe(II) enantiomers: syntheses and structures of ΛΔ/ΔΛ-Bis(Dihydridoborate) complexes},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {31},
	year = {2025},
	month = {FEB },
	type = {Article},
	abstract = {<p>
	In our effort to establish a direct synthetic approach for bis(dihydridoborate) complexes of first-row transition metals, we have investigated the reactivity of [Cp*Fe(dppe)Cl] (dppe =1,2-bis(diphenylphosphino)ethane) with Na[BH3L] (L =2-mercaptopyridine (mp) and 2-mercaptobenzothiazole (mbz)) that led to the formation of iron(II) dihydridoborate complexes, [Cp*Fe{kappa 3-S,H,H-(H2BH(L))}] 1 a-b (L=mp (1 a) and L=mbz (1 b)). Further, in an attempt to isolate the bis(dihydridoborate) complex of iron by the insertion of borane into the kappa 2-N,S-chelated iron complex, [(dppe)Fe{kappa 2-N,S-(mp)}2] (2), we have isolated and structurally characterized a rare example of dimeric iron bis(dihydridoborate) complex, [Fe{kappa 3-S,H,H-(H2BH(mp))}2]2, Lambda Delta/Delta Lambda-3 as pair of enantiomers. Interestingly, these enantiomers Lambda Delta/Delta Lambda-3 have two trans-[Fe{kappa 3-S,H,H-(H2BH(mp))}2] moieties bridged through sulfur atoms of 2-mercaptopyridinyl ligands, where the iron centres are hepta-coordinated. The natural bond-orbital (NBO) analyses of Lambda Delta-3 and Delta Lambda-3 show considerable electron donation from the filled sigma B-H bonding orbital to vacant dz2 \${{d}_{{z}\&lt;\^\&gt;{2}}}\$ orbital of iron with a substantial contribution from the hydrogen atoms. The localized orbital bonding analysis (LOBA) method suggests that all the iron centres are in +2 oxidation state.</p>
},
	keywords = {B-H activation, Bis(dihydridoborate), Enantiomer, Heptacoordinate, iron},
	issn = {0947-6539},
	doi = {10.1002/chem.202404469},
	author = {Kaur, Urminder and Gayen, Sourav and Sharma, Himanshu and Vanka, Kumar and Ghosh, Sundargopal}
}
