Asymmetric Azido−Copper(II) Bridges: Ferro- or Antiferromagnetic? Experimental and Theoretical Magneto−Structural Studies
Reaction of NaN3 with the [CuII(tn)]2+ ion (tn = 1,3-diaminopropane) in basic aqueous solution yields the azido-bridged complex of formula [Cu2(tn)2(N3)4] (1), which is characterized by X-ray crystallography. The structure of 1 is made up of dinuclear neutral complexes, of formula [Cu2(tn)2(N3)4], r...
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Veröffentlicht in: | Inorganic chemistry 2005-07, Vol.44 (15), p.5501-5508 |
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Sprache: | eng |
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Zusammenfassung: | Reaction of NaN3 with the [CuII(tn)]2+ ion (tn = 1,3-diaminopropane) in basic aqueous solution yields the azido-bridged complex of formula [Cu2(tn)2(N3)4] (1), which is characterized by X-ray crystallography. The structure of 1 is made up of dinuclear neutral complexes, of formula [Cu2(tn)2(N3)4], resulting from the assembling of two mononuclear units through two equivalent end-on azide bridges connecting asymmetrically two Cu(tn)(N3)2 entities. These dinuclear units are connected through two asymmetric end-to-end N3 bridges to form a chain of dimers. Magnetic measurements for compound 1 show weak antiferromagnetic exchange interactions between the Cu(II) ions. The magnetic data were modeled using the susceptibility expression derived for an alternating AF S = 1/2 chain. A very satisfactory fit over the whole temperature range was obtained with g = 2.1438(4), J 1 = −3.71(2) cm-1, and J 2 = −3.10(2) cm-1 (J 1 and J 2 are the singlet−triplet separations). This magnetic behavior differs from those observed for similar examples which were reported as having alternating ferro- and antiferromagnetic exchange interactions; thus, DFT calculations were done to understand the nature of the magnetic coupling in such asymmetric end-on and end-to-end N3 bridges. Theoretical results show that the double asymmetric end-on bridges produce antiferromagnetic coupling while the end-to-end ones can present ferro- or antiferromagnetic coupling depending on the copper coordination sphere. |
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ISSN: | 0020-1669 1520-510X |
DOI: | 10.1021/ic0504543 |