Anion‐Directed Template Synthesis and Hydrolysis of Mono‐Condensed Schiff Base of 1,3‐Pentanediamine and o ‐Hydroxyacetophenone in Ni II and Cu II Complexes
Bis( o ‐hydroxyacetophenone)nickel(II) dihydrate, on reaction with 1,3‐pentanediamine, yields a bis‐chelate complex [NiL 2 ] · 2H 2 O ( 1 ) of mono‐condensed tridentate Schiff baseligand HL {2‐[1‐(3‐aminopentylimino)ethyl]phenol}. The Schiff base has been freed from the complex by precipitating the...
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Veröffentlicht in: | European journal of inorganic chemistry 2008-07, Vol.2008 (21), p.3372-3381 |
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Sprache: | eng |
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Zusammenfassung: | Bis(
o
‐hydroxyacetophenone)nickel(II) dihydrate, on reaction with 1,3‐pentanediamine, yields a bis‐chelate complex [NiL
2
]
·
2H
2
O (
1
) of mono‐condensed tridentate Schiff baseligand HL {2‐[1‐(3‐aminopentylimino)ethyl]phenol}. The Schiff base has been freed from the complex by precipitating the Ni
II
as a dimethylglyoximato complex. HL reacts smoothly with Ni(SCN)
2
·
4H
2
O furnishing the complex [NiL(NCS)] (
2
) and with CuCl
2
·
2H
2
O in the presence of NaN
3
or NH
4
SCN producing [CuL(N
3
)]
2
(
3
) or [CuL(NCS)] (
4
). On the other hand, upon reaction with Cu(ClO
4
)
2
·
6H
2
O and Cu(NO
3
)
2
·
3H
2
O, the Schiff base undergoes hydrolysis to yield ternary complexes [Cu(hap)(pn)(H
2
O)]ClO
4
(
5
) and [Cu(hap)(pn)(H
2
O)]NO
3
(
6
), respectively (Hhap =
o
‐hydroxyacetophenone and pn = 1,3‐pentanediamine). The ligand HL undergoes hydrolysis also on reaction with Ni(ClO
4
)
2
·
6H
2
O or Ni(NO
3
)
2
·
6H
2
O to yield [Ni(hap)
2
] (
7
). The structures of the complexes
2
,
3
,
5
,
6
, and
7
have been confirmed by single‐crystal X‐ray analysis. In complex
2
, Ni
II
possesses square‐planar geometry, being coordinated by the tridentate mono‐negative Schiff base, L and the isothiocyanate group. The coordination environment around Cu
II
in complex
3
is very similar to that in complex
2
but here two units are joined together by end‐on, axial‐equatorial azide bridges to result in a dimer in which the geometry around Cu
II
is square pyramidal. In both
5
and
6
, the Cu
II
atoms display the square‐pyramidal environment; the equatorial sites being coordinated by the two amine groups of 1,3‐pentanediamine and two oxygen atoms of
o
‐hydroxyacetophenone. The axial site is coordinated by a water molecule. Complex
7
is a square‐planar complex with the Ni atom bonded to four oxygen atoms from two hap moieties. The mononuclear units of
2
and dinuclear units of
3
are linked by strong hydrogen bonds to form a one‐dimensional network. The mononuclear units of
5
and
6
are joined together to form a dimer by very strong hydrogen bonds through the coordinated water molecule. These dimers are further involved in hydrogen bonding with the respective counteranions to form 2‐D net‐like open frameworks. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) |
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ISSN: | 1434-1948 1099-0682 |
DOI: | 10.1002/ejic.200800186 |