首页> 外文期刊>Physical chemistry chemical physics: PCCP >Photogeneration of metastable side-on N2 linkage isomers in [Ru(NH3)5N2]Cl2, [Ru(NH3)5N2]Br2 and [Os(NH3)5N2]Cl2
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Photogeneration of metastable side-on N2 linkage isomers in [Ru(NH3)5N2]Cl2, [Ru(NH3)5N2]Br2 and [Os(NH3)5N2]Cl2

机译:[Ru(NH3)5N2] Cl2,[Ru(NH3)5N2] Br2和[Os(NH3)5N2] Cl2中亚稳的侧面N2键联异构体的光生

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摘要

Photogeneration of side-on N2 linkage isomers in [Ru(NH3)5N2]~(2+) and [Os(NH3)5N2]~(2+) is achieved by irradiation with λ = 325 nm of powder samples at T = 80 K and detected by the downshift of the v(N-N) vibration and by the heat release at elevated temperature due to the back switching of the side-on configuration to the ground state. The concentration of the transferred molecules is evaluated by the decrease of the area of the v(N-N) or 2v(N-N) vibrational bands. All characteristic changes between the linear Ru-N-N and side-on configuration are predicted by DFT calculations: the structure of the anion, shifts of the vibrations, electronic excitation energy, energetic position and sequence of the electronic orbitals, the potentials of the ground and relaxed metastable state with the activation energy, saddle points and energetic position of the minimum.
机译:在[Ru(NH3)5N2]〜(2+)和[Os(NH3)5N2]〜(2+)中侧向N2键合异构体的光生是通过在T = 80照射粉末样品的λ= 325 nm实现的由于侧向配置反向切换到基态,通过v(NN)振动的降档和高温释放的热量来检测K。通过减小v(N-N)或2v(N-N)振动带的面积来评估转移分子的浓度。通过DFT计算可以预测线性Ru-NN和侧面结构之间的所有特征变化:阴离子的结构,振动的位移,电子激发能,电子轨道的高能位置和顺序,地面和弛豫的亚稳态具有最小的活化能,鞍点和高能位置。

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