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Wang, G L; Lin, Y J; Berke, H; Jin, G X (2010). Two-step assembly of multinuclear metallacycles with half-sandwich Ir, Rh, and Ru fragments for counteranion encapsulation. Inorganic Chemistry, 49(5):2193-2201.

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Abstract

Two-step reactions of CP*M(mu-Cl)Cl](2) (M = Ir, Rh) and (p-cymene)Ru-(mu-Cl)Cl](2) with first AgOTf or AgPF6 and then pyridyl-substituted dionate ligands 3-(4-pyridyl)pentane-2,4-dione (L-1), 1-(4-pyridinyl)butane-1,3-dione (L-2), 1-(3-pyridinyl)butane-1,3-dione (LA resulted in the formation of the hexanuclear 48-membered metallacycles (Cp*Ir)(L-1)](6)center dot(OTf)(6) (1) and (Cp*Rh)(L-1)](6)center dot(OTf)(6) (2), the tetranuclear 28-membered metallacycle (Cp*Ir)(L-2)(4)center dot(OTf)(4) (3), and the 24-membered metallacycle (p-cymene)Ru(L-3)](4)center dot(OTf)(4) (4), as well as the hexanuclear 48-membered metallacycles (p-cymene)Ru(L-1)](6)(OTf)center dot(OTf)(5) (5) and {(p-cymene)Ru(L-1)](6)-(PF6)}center dot(PF6)(5) (6) showing encapsulation of the counteranions. Compounds 1-6 were characterized by single crystal X-ray analyses and revealed that these metallacycles constructed from half-sandwich metal corners and pyridyl-substituted diketone linkers formed large ring structures. In addition, when the couteranions of 5 and 6 were exchanged, the shapes and sizes of the host units (p-cymene)Ru(L-1)](6)(6+) underwent some self-adjustment to allow for accommodation of the different anionic guests. Weak hydrogen bonding of the type C(S)-F(O)center dot center dot center dot H-C(sp(3)) and P-F center dot center dot center dot H-C(sp(3)) and electrostatic interactions are considered the basic forces to establish the metallacyclic units in 5 and 6 with anion encapsulation. The found variation in the metallacyclic geometries was explained on the basis of a structural flexibility of the corner fragments, subtle changes in coordination geometries, and changes in the orientation of the coordinate vectors in the given ligands, as well as the dihedral angles between the two binding fragments (the chelate and the monodentate fragments) in the nonplanar ligands.

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
DDC:540 Chemistry
Language:English
Date:2010
Deposited On:23 Feb 2011 18:31
Last Modified:27 Nov 2013 19:44
Publisher:American Chemical Society
ISSN:0020-1669
Publisher DOI:10.1021/ic902011v
PubMed ID:20121071
Other Identification Number:ISI:000274626200024
Citations:Web of Science®. Times Cited: 15
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Scopus®. Citation Count: 17

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