Premium
Hierarchical, Lithium‐Templated Assembly of Helicate‐Type Complexes: How Versatile Is This Reaction?
Author(s) -
Albrecht Markus,
Fiege Marcel,
Baumert Miriam,
de Groot Marita,
Fröhlich Roland,
Russo Luca,
Rissanen Kari
Publication year - 2007
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200600852
Subject(s) - chemistry , lithium (medication) , catechol , cobalt , nickel , boron , zinc , stereochemistry , inorganic chemistry , organic chemistry , medicine , endocrinology
Catechol ligands that bear carbonyl functions such as esters or aldehydes in the 3‐position ( 1a – c ‐H 2 ) form triple‐stranded, helicate‐type complexes [Li 3 ( 1a – c ) 6 Ti 2 ] – with titanium(IV) and the corresponding double‐stranded compounds [Li 2 ( 1a – c ) 4 B 2 ] with boron(III) in hierarchical, lithium‐templatedprocesses. The related 8‐hydroxyquinoline ligands 2a , b ‐H can be used for the formation of similar complexes[Li 3 ( 2a , b ) 6 M 2 ] + with cobalt(II), nickel(II), or zinc(II). A prerequisite for the formation of the lithium‐bridged dimers is a negative charge of the mononuclear complexes, which are able to electrostatically attract the lithium cations and thus compensate the repulsion between the cations. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom