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New iodometallate(I) with in situ generated organic base derivatives as countercations (M+ = Ag+, Cu+)
Journal of Solid State Chemistry ( IF 3.2 ) Pub Date : 2018-09-27 , DOI: 10.1016/j.jssc.2018.09.035
Rong-Yan Wang , Xiao Zhang , Jie-Hui Yu , Ji-Qing Xu

By employing the solvothermal in situ N-alkylation of organic bases with alcohol molecules, four new organically templated iodometallates as [L1][Ag2I4] (L12+ = 1,1,4,4-tetramethyl-1λ4,4λ4-piperazinium) 1, [L2]1.5[AgI4] (L22+ = 1,4-dibenzyl-1λ4,4λ4-diazabicyclo[2.2.2]octanium) 2, [L2]1.5[CuI4] 3 and [L3][CuI3] (L32+ = 4,4'-bis(3-methyl-1H-3λ4-imidazol-1-yl)−1,1'-biphenylium) 4 were obtained. In 1, the in situ substitution and N-alkylation of 1,4-bis(pyridin-4-ylmethyl)piperazine (L1') with CH3OH has occurred, producing L12+. Templated by L12+, Ag+ and I- aggregate into a chained iodoargentate, which can be described as a linear arrangement of AgI4 tedrahedra by sharing the edges. 2 and 3 are isostructural. In 2 and 3, the in situ N-alkylation of 1,4-diazabicyclo[2,2,2]octane (L2') with phenylmethanol has occurred, generating L22+. Templated by L22+, Ag+ (or Cu+) and I- aggregate into a mononuclear iodometallate with a tetrahedral structure. In 4, the in situ N-alkylation of 4,4'-di(1H-imidazol-1-yl)−1,1'-biphenyl (L3') with CH3OH has occurred, creating L32+. Templating by L32+, Cu+ and I- aggregate into a mononuclear iodocuprate(I) with a planar trigonal structure. The photoluminescence analysis reveals that (i) at the room temperature, only 1 emits light (λem = 550 nm); (ii) at the low temperature, 4 is found to possess the photoluminescence property (λem = 546 nm at 77 K) with a ms-grade lifetime (τ = 4.915 ms).



中文翻译:

具有原位生成的有机碱衍生物作为抗衡阳离子的新型碘金属盐(I)(M + = Ag +,Cu +

通过采用溶剂热在原位Ñ与醇分子,四个新的有机模板iodometallates如[L1] [银有机碱烷基化24 ](L1 2+ = 1,1,4,4-四甲基1λ 4,4λ 4 -piperazinium)1,[L2] 1.5 [碘化银4 ](L2 2+ = 1,4-二苄基1λ 4,4λ 4二氮杂双环[2.2.2] octanium)2,[L2] 1.5 [的CuI 4 ] 3和[L3] [的CuI 3 ](L3 2+ = 4,4'-双(3-甲基-1H-3λ 4获得了-咪唑-1-基)-1,1'-联苯铵)4。在1中,发生了用CH 3 OH原位取代和1,4-双(吡啶-4-基甲基)哌嗪(L1')的N-烷基化,产生了L1 2+。由L1模板2+,银+和我-聚集成链式iodoargentate,其可以被描述为碘化银的线性排列4通过共享边缘tedrahedra。23是同构的。在23中原位N1,4-二氮杂双环[2,2,2]辛烷(L2')与苯基甲醇发生了烷基化反应,生成了L2 2+。通过L2模板2+,银+(或Cu +)和I -骨料与四面体结构的单核iodometallate。在4中,发生了用CH 3 OH进行的4,4'-二(1H-咪唑-1-基)-1,1'-联苯(L3')的原位N-烷基化反应,生成了L3 2+。通过L3模板2+,铜+和我-聚集成的单核iodocuprate(I)具有平面三角结构。光致发光分析表明(i)在室温下,只有1发光(λem = 550  nm); (ii)在低温下,发现4具有光致发光特性(在77 K时λem = 546  nm  ),寿命为ms级(τ= 4.915 ms)。

更新日期:2018-09-28
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