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Acta chemica Scandinavica最新文献

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Traversing the Space of the Oral-Written Continuum: Medially Connotative Back-Referring Formulae in Landnámabók 穿越口语-书面语连续体的空间:Landnámabók中隐含的回指公式
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116627
Slavica Ranković
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引用次数: 0
Letters from Kings: Epistolary Communication in the Kings’ Sagas (until c. 1150) 国王的书信:国王传奇中的书信交流(直到约1150年)
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116622
Jonas Wellendorf
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引用次数: 0
Creating Absence: The Representation of Writing in Early Histories of the North 创造缺席:早期北方历史中文字的表现
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116620
Aidan Conti
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引用次数: 0
Tracing Scribal Centres in Medieval Norway 追溯中世纪挪威的抄写中心
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116621
Å. Ommundsen
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引用次数: 0
Literacy Studies: Past, Present, and Future 识字研究:过去、现在和未来
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116618
L. Melve
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引用次数: 0
Letters, Networks, and Public Opinion in Medieval Norway (1024-1263) 中世纪挪威的信件、网络和公众舆论(1024-1263)
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116623
L. Melve
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引用次数: 0
Gyrðir á lykil (Gyrðir owns the key): Materialized Moments of Communication in Runic Items from Medieval Bergen gyr æ ir <e:1> lykil (gyr æ ir拥有钥匙):中世纪卑尔根的符文物品中的物化交流时刻
Pub Date : 2019-01-01 DOI: 10.1484/m.as-eb.5.116624
Kristel Zilmer
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引用次数: 1
Front Matter (“Table of Contents”, “Preface”) 封面(“目录”、“前言”)
Pub Date : 2013-06-24 DOI: 10.1484/m.as-eb.5.122655
M. Bordo, Athanasios Orphanides
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引用次数: 0
Platinum(II)Benzophenone Imine Complexes and the Crystal Structure of trans-(N,N)-(Benzophenoneimine)chloro-[2-(1-imino-1-phenylmeth yl)phenyliodo]-platinum(II)-Acetone(2/1) 铂(II)二苯甲酮亚胺配合物及反式-(N,N)-(二苯甲酮亚胺)氯-[2-(1-亚胺-1-苯基甲基)苯基碘]-铂(II)-丙酮(2/1)的晶体结构
Pub Date : 1999-12-01 DOI: 10.3891/ACTA.CHEM.SCAND.53-1069
L. Groendahl, J. Josephsen, Rikke Christina Mattsson Bruun, S. Larsen
Syntheses and characterisation by H-1 NMR and IR of the platinum(II) complexes [PtI2(Ph2C=NH)(2)], [PtCl2(Ph2C=NH)(2)], [PtCl(Ph(Ph-H)C=NH)-(NH2CH2CH2NH2)] and trans-(N,N)-[PtCl(Ph(Ph-H)C=NH)(Ph2C=NH)] are described. Absorption and emission spectra at room temperature for the latter complex are reported. The crystal structure of trans-(N,N)[PtCl(Ph(Ph-H)C=NH)(Ph2C=NH)] . 1/2{(CH3)(2)CO} was determined by X-ray diffraction methods. Space group C2/c, a = 14.318(4) Angstrom, b = 22.854(4) Angstrom. c = 15.212(3) Angstrom and beta = 108.42(2)degrees using 10 368 reflections in the refinement of 291 parameters gave R = 0.037 and wR2 = 0.074 (for all data). The ligands surround platinum in a planar configuration with bond lengths of Pt-Cl 2.404(1) Angstrom, Pt-N (monodentate imine ligand) 2.004(3) Angstrom, Pt-N (bidentate imine ligand) 1.979(3) Angstrom and Pt-C 1.988(3) Angstrom. The chemical shifts in the H-1 NMR spectrum of trans-(N,N)-[PtCl(Ph(Ph-H)C=NH)(Ph2C=NH)] (in CDCl3) display variations with concentration of the complex that indicate dimerisation. The dimerisation constant was determined from the change in chemical shift for the NH proton of the ortho-metalated ligand, K = 1.25(4) M-1 at 300 K. The structure of the dimer in solution is proposed to resemble one of the types of interactions that are encountered between platinum complexes in the solid state.
描述了铂(II)配合物[PtI2(Ph2C=NH)(2)]、[PtCl2(Ph2C=NH)(2)]、[PtCl(Ph(Ph- h)C=NH)-(NH2CH2CH2NH2)]和反式-(N,N)-[PtCl(Ph(Ph- h)C=NH)(Ph2C=NH)]的合成及H-1 NMR和IR表征。报道了后一种配合物在室温下的吸收光谱和发射光谱。反式-(N,N)的晶体结构[PtCl(Ph(Ph- h)C=NH)(Ph2C=NH)]。用x射线衍射法测定了1/2{(CH3)(2)CO}。空间群C2/c, a = 14.318(4)埃,b = 22.854(4)埃。c = 15.212(3)埃,beta = 108.42(2)度,在291个参数的细化中使用10 368个反射,R = 0.037, wR2 = 0.074(对于所有数据)。配体围绕铂呈平面构型,键长分别为Pt-Cl 2.404(1)埃、Pt-N(单齿亚胺配体)2.004(3)埃、Pt-N(双齿亚胺配体)1.979(3)埃和Pt-C 1.988(3)埃。反式-(N,N)-[PtCl(Ph(Ph- h)C=NH)(Ph2C=NH)] (CDCl3)的H-1核磁共振谱的化学位移显示出配合物浓度的变化,表明二聚化。二聚化常数由邻金属化配体的NH质子在300 K时的化学位移变化确定,K = 1.25(4) M-1。溶液中二聚体的结构类似于固态铂配合物之间的相互作用类型之一。
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引用次数: 5
Experimental and theoretical investigation of the UV spectrum and kinetics of the aminomethyl radical, .CH2NH2 氨基甲基自由基。ch2nh2紫外光谱和动力学的实验和理论研究
Pub Date : 1999-11-01 DOI: 10.3891/ACTA.CHEM.SCAND.53-1054
T. I. Jansen, I. Trabjerg, S. Rettrup, P. Pagsberg, A. Sillesen
The aminomethyl radical was produced by the reaction F-. + CH3NH2 --> HF + (CH2NH2)-C-., which was initiated by pulse radiolysis of CH3NH2-SF6 mixtures. The ultraviolet absorption spectrum of CH2NH2 was recorded on a timescale of 2 mu s using a gated optical multichannel analyzer. The vibronic structure observed in the range 270-380 nm was analyzed by comparison with the results Of ab initio calculations. Kinetics of the self-reaction 2(.)CH(2)NH(2) --> products was studied by monitoring the transient absorption of (CH2NH2)-C-. at 319.5 nm. A value of k = 8.1 x 10(-11) cm(3) molecule(-1) s(-1) was derived from the observed second-order kinetics combined with an estimated yield of the radical. In the presence of oxygen the decay rate was found to increase in accordance with the reaction (CH2NH2)-C-. + O-2 --> products proceeding with a rate constant of 7.8(8) x 10(-11) cm(3) molecule(-1) s(-1).
氨基甲基自由基由F-反应产生。+ ch3nh2 -> hf + (ch2nh2)- c -。,由脉冲辐射分解CH3NH2-SF6混合物引发。利用门控光多通道分析仪在2 μ s的时间尺度上记录了CH2NH2的紫外吸收光谱。通过与从头计算结果的比较,分析了在270 ~ 380 nm范围内观察到的振动结构。通过监测(CH2NH2)- c -的瞬态吸收,研究了自反应2(.)CH(2)NH(2) ->产物的动力学。在319.5 nm。根据观察到的二级动力学结合自由基的估计产率,得出k = 8.1 x 10(-11) cm(3)分子(-1)s(-1)的值。在有氧存在的情况下,发现衰变速率随着(CH2NH2)- c -的反应而增加。+ O-2 ->产物的反应速率常数为7.8(8)× 10(-11) cm(3)分子(-1)s(-1)。
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引用次数: 7
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Acta chemica Scandinavica
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