Spin State of the pH-Sensitive Cobalt(II) Complex with the Bis(pyrazol-3-yl)pyridine-Based Ligand

IF 1.1 3区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
E. S. Safiullina, I. A. Nikovskiy, Yu. V. Nelyubina
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引用次数: 0

Abstract

New cobalt(II) complex [Co(L)2](ClO4)2 is synthesized by the reaction of 2,6-bis(pyrazol-3-yl)pyridine (L) containing capable of deprotonating hydroxy groups with cobalt(II) perchlorate hexahydrate in deuterated methanol in a tube for NMR spectroscopy. A possibility of the new complex to undergo in situ reversible deprotonation under the action of 1,8-diazabicyclo[5.4.0]undec-7-ene is demonstrated. As found by the approach based on an analysis of changing chemical shifts in the 1H NMR spectra with temperature, the synthesized complex exists in the high-spin state both before and after complete deprotonation in a temperature range of 200–325 K. The X-ray diffraction (XRD) data of the completely deprotonated complex [Co(L-2H)2](DBU+H)2 (CIF file CCDC no. 2448321) indicate that the high-spin state of the complex is retained in the crystal as well.

Abstract Image

Abstract Image

ph敏感性钴(II)配合物与双(吡唑-3-基)吡啶基配体的自旋态
以2,6-二(吡唑-3-基)吡啶(L)与六水高氯酸钴(II)在氘化甲醇中反应合成了新的钴(II)配合物[Co(L)2](ClO4)2。在1,8-二氮杂环[5.4.0]十一-7-烯的作用下,新配合物可能发生原位可逆去质子化。通过对1H NMR谱随温度变化的化学位移分析发现,在200-325 K温度范围内,合成的配合物在完全去质子化前后均处于高自旋态。完全去质子配合物[Co(L-2H)2](DBU+H)2 (CIF文件CCDC号)的x射线衍射(XRD)数据。2448321)表明配合物的高自旋态也保留在晶体中。
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来源期刊
Russian Journal of Coordination Chemistry
Russian Journal of Coordination Chemistry 化学-无机化学与核化学
CiteScore
2.40
自引率
15.80%
发文量
85
审稿时长
7.2 months
期刊介绍: Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.
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