Synthesis and reactivity of organolanthanide complexes containing phenothiazine ligand toward carbodiimide and isothiocyanate
Four new organolanthanide phenothiazine complexes were synthesized, and their reactivities toward carbodiimide or isothiocyanate were investigated, indicating that carbodiimide or isothiocyanate readily mono-inserts into the lanthanide–nitrogen bonds to give the corresponding insertion products. All...
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Published in | Journal of organometallic chemistry Vol. 690; no. 21; pp. 4926 - 4932 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.11.2005
|
Subjects | |
Online Access | Get full text |
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Summary: | Four new organolanthanide phenothiazine complexes were synthesized, and their reactivities toward carbodiimide or isothiocyanate were investigated, indicating that carbodiimide or isothiocyanate readily mono-inserts into the lanthanide–nitrogen bonds to give the corresponding insertion products. All the reactions provide an alternative synthetic strategy for the modification of the phenothiazine ligand.
The synthesis and reactivity of new lanthanocene complexes incorporating phenothiazine ligand are described. The reaction of phenothiazine (HPtz) with
n
BuLi in THF and subsequently with 1 equiv. of (C
5H
5)
2LnCl(THF) gave the original complexes (C
5H
5)
2LnPtz(THF) (Ln
=
Yb(
1), Er(
2), Dy(
3), Y(
4)). Treatment of complexes
1–
4 with
N,
N′-diisopropylcarbodiimide results in mono-insertion of carbodiimide into the Ln–N(Ptz)-bond to yield the corresponding guanidinates (C
5H
5)
2Ln[(
i
PrN)
2C(Ptz)] (Ln
=
Yb (
5), Er (
6), Dy (
7), Y(
8)). Further investigations indicate that phenyl isothiocyanate react with complexes
1 and
4, giving the correspondent insertion products (C
5H
5)
2Ln[SC(Ptz)NPh](THF) (Ln
=
Yb(
9), Y(
10)). All these complexes were characterized by elemental analysis and spectroscopic properties. The structures of complexes
2,
5 and
9 were also determined by the X-ray single crystal diffraction analysis. All these reactions provide a new strategy for introducing a functional substituent at the nitrogen atom of phenothiazine via forming a new C–N(ring) bond. |
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ISSN: | 0022-328X 1872-8561 |
DOI: | 10.1016/j.jorganchem.2005.08.005 |