KOPS - The Institutional Repository of the University of Konstanz

Aqueous-phase synthesis of di-(η<sup>5</sup>-cyclopentadienyl)salicylato-anddi-(η<sup>5</sup>-cyclopentadienyl)phthalatotitanium(IV) complexes

Aqueous-phase synthesis of di-(η5-cyclopentadienyl)salicylato-anddi-(η5-cyclopentadienyl)phthalatotitanium(IV) complexes

Type of Publication: Journal article
URI (citable link): http://nbn-resolving.de/urn:nbn:de:bsz:352-239838
Author: Meirim, Maria G.; Neuse, Eberhard W.; Rhemtula, Mariam; Schmitt, Siegfried; Brintzinger, Hans-Herbert
Year of publication: 1988
Published in: Transition Metal Chemistry ; 13 (1988), 4. - pp. 272-276. - ISSN 0340-4285. - eISSN 1572-901X
DOI (citable link): https://dx.doi.org/10.1007/BF01025672
Summary:
Di-(η5-cyclopentadienyl)dichlorotitanium(IV) reacts with salicylic acid or some of its ring-substituted derivatives in aqueous medium in the presence of alkali carbonate, giving (substituted) di-(η5-cyclopentadienyl)-salicylatotitanium(IV) complexes(3). Analogously, although less efficaciously, the dichlorotitanium compound reacts with phthalic acid to give the phthalato complex(5), and with dipicolinic acid to yield the pyridinedicarboxylato compound(7). Meticulous control of the experimental conditions is necessary to minimize hydrolytic side reactions. The product complexes(3) and(5) can be recrystallized from chloroform, in which they dissolve completely when freshly prepared; prolonged storage at ambient temperature causes reductions in solubility. I.r. and n.m.r. spectroscopic features of the product complexes are presented.
Subject (DDC): 540 Chemistry
Link to License: Terms of use

Cite This

Files in this item

[PDF]
Name: 10.1007_BF01025672Meirim.pdf
Size: 495.3Kb
Format: PDF
View/Open
Checksum: MD5:e23e7d5bb9ce11eab3cbd6d3f58ed6c9

MEIRIM, Maria G., Eberhard W. NEUSE, Mariam RHEMTULA, Siegfried SCHMITT, Hans-Herbert BRINTZINGER, 1988. Aqueous-phase synthesis of di-(η5-cyclopentadienyl)salicylato-anddi-(η5-cyclopentadienyl)phthalatotitanium(IV) complexes. In: Transition Metal Chemistry. 13(4), pp. 272-276. ISSN 0340-4285. eISSN 1572-901X. Available under: doi: 10.1007/BF01025672

@article{Meirim1988Aqueo-23983, title={Aqueous-phase synthesis of di-(η5-cyclopentadienyl)salicylato-anddi-(η5-cyclopentadienyl)phthalatotitanium(IV) complexes}, year={1988}, doi={10.1007/BF01025672}, number={4}, volume={13}, issn={0340-4285}, journal={Transition Metal Chemistry}, pages={272--276}, author={Meirim, Maria G. and Neuse, Eberhard W. and Rhemtula, Mariam and Schmitt, Siegfried and Brintzinger, Hans-Herbert} }

Schmitt, Siegfried Meirim, Maria G. 1988 Brintzinger, Hans-Herbert 2013-08-13T08:15:47Z 2013-08-13T08:15:47Z Rhemtula, Mariam Neuse, Eberhard W. Schmitt, Siegfried Neuse, Eberhard W. Meirim, Maria G. eng Aqueous-phase synthesis of di-(η<sup>5</sup>-cyclopentadienyl)salicylato-anddi-(η<sup>5</sup>-cyclopentadienyl)phthalatotitanium(IV) complexes terms-of-use Di-(η<sup>5</sup>-cyclopentadienyl)dichlorotitanium(IV) reacts with salicylic acid or some of its ring-substituted derivatives in aqueous medium in the presence of alkali carbonate, giving (substituted) di-(η<sup>5</sup>-cyclopentadienyl)-salicylatotitanium(IV) complexes(3). Analogously, although less efficaciously, the dichlorotitanium compound reacts with phthalic acid to give the phthalato complex(5), and with dipicolinic acid to yield the pyridinedicarboxylato compound(7). Meticulous control of the experimental conditions is necessary to minimize hydrolytic side reactions. The product complexes(3) and(5) can be recrystallized from chloroform, in which they dissolve completely when freshly prepared; prolonged storage at ambient temperature causes reductions in solubility. I.r. and n.m.r. spectroscopic features of the product complexes are presented. Rhemtula, Mariam Brintzinger, Hans-Herbert Transition Metal Chemistry ; 13 (1988), 4. - S. 272-276

Downloads since Oct 1, 2014 (Information about access statistics)

10.1007_BF01025672Meirim.pdf 291

This item appears in the following Collection(s)

Search KOPS


Browse

My Account