Iron(ii) thio- and selenocyanate coordination networks containing 3,3′-bipyridineElectronic supplementary information (ESI) available. CCDC reference numbers 818774–818781. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c1ce05352c

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Title: Iron(ii) thio- and selenocyanate coordination networks containing 3,3′-bipyridineElectronic supplementary information (ESI) available. CCDC reference numbers 818774–818781. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c1ce05352c
Authors: Christopher J. Adams1, Mairi F. Haddow1, David J. Harding2, Thomas J. Podesta1, Rachel E. Waddington1
Source: CrystEngComm. Jul2011, Vol. 13 Issue 15, p4909-4914. 6p.
Subjects: Iron compounds, Crystallography, Chemical reactions, Bipyridine, Solvents, Methanol, Monomers, Stoichiometry, Acetonitrile
Abstract: A number of different compounds have been synthesised by reaction of solutions containing Fe(NCE)2(E = S, Se) with solutions containing 3,3′-bipyridine. When the solvent used is methanol, the products are the monomeric compounds trans-{Fe(NCS)2(3,3′-bipy)2(MeOH)2} 1or trans-{Fe(NCSe)2(3,3′-bipy)2(MeOH)2} 2, but when acetonitrile is used the layered coordination network {Fe(NCS)2(3,3′-bipy)2} 3or doubly interpenetrated coordination network {Fe(NCSe)2(3,3′-bipy)2} 4is formed instead. Using methanol to dissolve the Fe(NCE)2and CHX3(X = Cl, Br) to dissolve the 3,3′-bipyridine yields solvated coordination networks of stoichiometry {Fe(NCE)2(3,3′-bipy)2}·2CHX3. The crystal structures of all of these compounds except 4are presented. [ABSTRACT FROM AUTHOR]
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  Data: Iron(ii) thio- and selenocyanate coordination networks containing 3,3′-bipyridineElectronic supplementary information (ESI) available. CCDC reference numbers 818774–818781. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c1ce05352c
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  Data: A number of different compounds have been synthesised by reaction of solutions containing Fe(NCE)2(E = S, Se) with solutions containing 3,3′-bipyridine. When the solvent used is methanol, the products are the monomeric compounds trans-{Fe(NCS)2(3,3′-bipy)2(MeOH)2} 1or trans-{Fe(NCSe)2(3,3′-bipy)2(MeOH)2} 2, but when acetonitrile is used the layered coordination network {Fe(NCS)2(3,3′-bipy)2} 3or doubly interpenetrated coordination network {Fe(NCSe)2(3,3′-bipy)2} 4is formed instead. Using methanol to dissolve the Fe(NCE)2and CHX3(X = Cl, Br) to dissolve the 3,3′-bipyridine yields solvated coordination networks of stoichiometry {Fe(NCE)2(3,3′-bipy)2}·2CHX3. The crystal structures of all of these compounds except 4are presented. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of CrystEngComm is the property of Royal Society of Chemistry and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – TitleFull: Iron(ii) thio- and selenocyanate coordination networks containing 3,3′-bipyridineElectronic supplementary information (ESI) available. CCDC reference numbers 818774–818781. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c1ce05352c
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