Intramolecular N–H ⋯ X–Ir (X = H, F) hydrogen bonding in metal complexes
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002573
Reference11 articles.
1. An NMR method for distinguishing classical from nonclassical structures in transition metal polyhydrides
2. .eta.2-Dihydrogen on the brink of homolytic cleavage: trans-[Os(H.cntdot..cntdot..cntdot.H)H(PEt2CH2CH2PEt2)2]+ has spectroscopic and chemical properties between those of the isoelectronic complexes trans-[OsH(PPh2CH2CH2PPh2)2(.eta.2-H2)]+ and ReH3(PPh2CH2CH2PPh2)2
3. Assessment of the "T1 criterion" for distinguishing between classical and nonclassical transition-metal hydrides: hydride relaxation rates in tris(triarylphosphine)osmium tetrahydrides and related polyhydrides
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