首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Cross-linking of cyanide magnetic coordination polymers by rational insertion of formate, cyanide or azide
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Cross-linking of cyanide magnetic coordination polymers by rational insertion of formate, cyanide or azide

机译:通过合理插入甲酸盐,氰化物或叠氮化物的交联氰化物磁共配位聚合物

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摘要

Carefully selected molecular bridging ligands formate, cyanide and azide, that are known to transmit strong magnetic interactions, have been successfully inserted into the {[Mn ~(II) (H _(2) O) _(2) ] _(2) [Nb ~(IV) (CN) _(8) ]·4H _(2) O} _( n ) ( Mn _(2) Nb ) ferrimagnetic parent framework, resulting in the additional molecular bridging of the two Mn ~(II) centres in three new coordination polymers: {(NH _(4) )[(H _(2) O)Mn ~(II) -(μ-HCOO)-Mn ~(II) (H _(2) O)][Nb ~(IV) (CN) _(8) ]·3H _(2) O} _( n ) Mn _(2) NbHCOO , {(NH _(4) )[(NH _(3) )Mn ~(II) -(μ-CN)-Mn ~(II) (H _(2) O)][Nb ~(IV) (CN) _(8) ]·2H _(2) O} _( n ) Mn _(2) NbCN and {(NH _(4) )[(H _(2) O)Mn ~(II) -(μ-N _(3) )-Mn ~(II) (H _(2) O)][Nb ~(IV) (CN) _(8) ]·3H _(2) O} _( n ) Mn _(2) NbN _(3) . The extra bridging ligands cross-linking the two Mn ~(II) centers strongly influence the long-range ferrimagnetic order of the Nb ~(IV) –CN–Mn ~(II) parent framework by introducing competing antiferromagnetic interactions. The values of the J _(MnMn) constants were obtained by fitting the magnetic properties of the Mo ~(IV) congeners {(NH _(4) )[(H _(2) O)Mn ~(II) -(μ-HCOO)-Mn ~(II) (H _(2) O)][Mo ~(IV) (CN) _(8) ]·3H _(2) O} _( n ) Mn _(2) MoHCOO , {(NH _(4) )[(NH _(3) )Mn ~(II) -(μ-CN)-Mn ~(II) (H _(2) O)][Mo ~(IV) (CN) _(8) ]·2H _(2) O} _( n ) Mn _(2) MoCN and {(NH _(4) )[(H _(2) O)Mn ~(II) -(μ-N _(3) )-Mn ~(II) (H _(2) O)][Mo ~(IV) (CN) _(8) ]·3H _(2) O} _( n ) Mn _(2) MoN _(3) , where the paramagnetic Nb ~(IV) was substituted by the diamagnetic Mo ~(IV) , thus disabling the long-range magnetic ordering of the CN-framework. Our strategy demonstrates how chemists can control the magnetic behavior of molecular magnets by subtle and rational structural modification based on chemical knowledge.
机译:仔细选择的分子桥接配体甲酸盐,氰化物和叠氮化物,已知将强磁相互作用传递到{[Mn〜(II)(H _(2)O)_(2)] _(2) [Nb〜(IV)(CN)_(8)]·4H _(2)o} _(n)(Mn _(2)Nb)亚铁尾母框架,导致额外的分子桥接两个Mn〜( II)三种新的配位聚合物中的中心:{(NH _(4))[(H _(2)O)Mn〜(II) - (μ-HCOO)-MN〜(II)(H _(2)o) )] [Nb〜(iv)(cn)_(8)]·3h _(2)o} _(n)mn _(2)nbhcoo,{(nh _(4))[(nh _(3) )Mn〜(ii) - (μ-cn)-mn〜(ii)(h _(2)o)] [nb〜(iv)(cn)_(8)]·2h _(2)o} _ (n)Mn _(2)Nbcn和{(NH _(4))[(H _(2)O)Mn〜(II) - (μ-n _(3))-mn〜(ii)(h _(2)o)] [Nb〜(iv)(cn)_(8)]·3h _(2)o} _(n)mn _(2)nbn _(3)。交联两个Mn〜(II)中心的额外桥接配体通过引入竞争的反铁磁相互作用而强烈影响NB〜(IV)-CN-MN〜(II)级框架的远程Ferrimagetic阶。通过拟合Mo〜(IV)Congeners的磁性(NH _(4))[(H _(2))Mn〜(II) - (μ)来获得J _(MNMN)常数的值。(μ -HCOO)-MN〜(II)(H _(2)O)] [Mo〜(IV)(CN)_(8)]·3H _(2)O} _(n)Mn _(2)MoHCOO ,{(NH _(4))[(NH _(3))Mn〜(II) - (μ-CN)-MN〜(II)(H _(2)O)] [Mo〜(IV)( CN)_(8)]·2H _(2)o} _(n)Mn _(2)mocn和{(nh _(4))[(h _(2)o)mn〜(ii) - ( μ-n _(3))-mn〜(ii)(h _(2)o)] [mo〜(iv)(cn)_(8)]·3h _(2)o} _(n)mn _(2)MON _(3),其中顺磁Nb〜(iv)被二磁磁阻〜(iv)取代,从而禁用CN框架的远程磁化。我们的策略表明了化学家通过基于化学知识的微妙和合理的结构改性如何控制分子磁体的磁性。

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