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Crystal structure of bis­(azido-κN)bis­[2,5-bis­(pyridin-2-yl)-1,3,4-thia­diazole-κ2N2,N3]nickel(II)

Identifieur interne : 000050 ( Main/Exploration ); précédent : 000049; suivant : 000051

Crystal structure of bis­(azido-κN)bis­[2,5-bis­(pyridin-2-yl)-1,3,4-thia­diazole-κ2N2,N3]nickel(II)

Auteurs : Abdelhakim Laachir [Maroc] ; Fouad Bentiss [Maroc] ; Salaheddine Guesmi [Maroc] ; Mohamed Saadi [Maroc] ; Lahcen El Ammari [Maroc]

Source :

RBID : PMC:4384553

Abstract

Reaction of 2,5-bis­(pyridin-2-yl)-1,3,4-thia­diazole and sodium azide with nickel(II) triflate yielded the mononuclear title complex, [Ni(N3)2(C12H8N4S)2]. The NiII ion is located on a centre of symmetry and is octa­hedrally coordinated by four N atoms of the two bidentate heterocyclic ligands in the equatorial plane. The axial positions are occupied by the N atoms of two almost linear azide ions [N—N—N = 178.8 (2)°]. The thia­diazole and pyridine rings of the heterocyclic ligand are almost coplanar, with a maximum deviation from the mean plane of 0.0802 (9) Å. The cohesion of the crystal structure is ensured by π–π inter­actions between parallel pyridine rings of neighbouring mol­ecules [centroid-to-centroid distance = 3.6413 (14) Å], leading to a layered arrangement of the mol­ecules parallel to (001).


Url:
DOI: 10.1107/S2056989015000201
PubMed: 25878837
PubMed Central: 4384553


Affiliations:


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,
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<sup>2</sup>
<italic>N</italic>
<sup>2</sup>
,
<italic>N</italic>
<sup>3</sup>
]nickel(II)</title>
<author>
<name sortKey="Laachir, Abdelhakim" sort="Laachir, Abdelhakim" uniqKey="Laachir A" first="Abdelhakim" last="Laachir">Abdelhakim Laachir</name>
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<p>Reaction of 2,5-bis­(pyridin-2-yl)-1,3,4-thia­diazole and sodium azide with nickel(II) triflate yielded the mononuclear title complex, [Ni(N
<sub>3</sub>
)
<sub>2</sub>
(C
<sub>12</sub>
H
<sub>8</sub>
N
<sub>4</sub>
S)
<sub>2</sub>
]. The Ni
<sup>II</sup>
ion is located on a centre of symmetry and is octa­hedrally coordinated by four N atoms of the two bidentate heterocyclic ligands in the equatorial plane. The axial positions are occupied by the N atoms of two almost linear azide ions [N—N—N = 178.8 (2)°]. The thia­diazole and pyridine rings of the heterocyclic ligand are almost coplanar, with a maximum deviation from the mean plane of 0.0802 (9) Å. The cohesion of the crystal structure is ensured by π–π inter­actions between parallel pyridine rings of neighbouring mol­ecules [centroid-to-centroid distance = 3.6413 (14) Å], leading to a layered arrangement of the mol­ecules parallel to (001).</p>
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