Studies on organolanthanide complexes .58. Syntheses of 1,1'-(3-oxa-pentamethylene)dicyclopentadienyl divalent organolanthanides (Ln=Sm, Yb) and X-ray molecular structure of O(CH2CH2C5H4)(2)Yb(DME)

The compounds O(CH2CH2C5H4)(2)Ln(THF)(2) [Ln = Sm(1), Yb(2)] were synthesized by the reduction of O(CH2CH2C5H4)(2)LnCl with sodium metal in tetrahydrofuran (THF) at room temperature. Recrystallization of 2 from dimethoxyethane (DME) produced the single-crystal O(CH2CH2C5H4)(2)Yb(DME) (3) whose structure has been determined by an X-ray diffraction study. The crystals are orthorhombic, space group Pcab, with a = 14.168(4), b = 13.541(6), c = 19.314(8) Angstrom, Z = 8, D-calc. = 1.66 g cm(-3).

YAG：Er晶体中的自饱和跃迁和激光波长红移

用提拉法生长出ＹＡＧ：Ｅｒ晶体，测定和分析了晶体的晶胞参数。讨论了￣２Ｈ＿（１１／２），￣４Ｓ＿（３／２），￣４Ｆ＿（９／２）能级的发光与猝灭，￣４Ｉ＿（１１／２）→￣４Ｉ＿（１３／２）自饱和跃迁的变化规律及激光波长红移的有关因素。

多功能Nd：YAG激光牙科治疗机及临床应用

报导一种“多功能Ｎｄ：ＹＡＧ激光牙科治疗机”应用于临床，对龋齿、牙本质过敏、牙龈炎、牙周炎、冠周炎等口腔疾病的治疗，取得较满意的效果．

SYNTHESES OF (C4H7OCH2C5H4)(2)LNCL (LN=ND, GD, DY, YB) AND CRYSTAL-STRUCTURE OF (C4H7OCH2C5H4)(2)DYCL

The reaction of lanthanide trichlorides with sodium tetrahydrofurfurylcyclopentadienyl in THF afforded bis(tetrahydrofurfurylcyclopentadienyl)lanthanide chloride complexes (C4H7OCH2C5H4),LnCl (Ln = Nd, Gd, Dy, Yb). All of the complexes were characterized

A NEW METHOD FOR THE SYNTHESIS OF LN(ETA-6-C6ME6)(ALCL4)3 (LN=ND, SM, GD, YB), AND THE X-RAY CRYSTAL-STRUCTURE OF YB(ETA-6-C6ME6)(ALCL4)3.MEC6H5

A series of neutral eta6-C6Me6 complexes of lanthanide elements Ln(176-C6Me6)(AlCl4)3 . MeC6H5(Ln = Nd, Sm, Gd, Yb) has been prepared directly in good yields from the reaction of LnCl3, AlCl3 and C6Me6 in toluene. The complexes have been characte

SYNTHESIS AND CRYSTAL-STRUCTURE OF [LI(THF)4][((T)BUCP)YB(NPH2)3]

The title complex [Li(THF)4] [(tBuCp)Yb(NPh2)3] was synthesized by the reaction of t-butylcyclopentadienyl ytterbium dichloride with 2 equivalents of LiNPh2 in THF, hexane, and toluene at -78-degrees-C. The complex was characterized by elemental analysis,

［Li（THF）_4］［（t－BuCp）Yb（NPh_2）_3］的合成及晶体结

合成了标题配合物［Ｌｉ（ＴＨＦ）＿４］［ｔ－ＢｕＣｐ）Ｙｂ（ＮＰｈ＿２）＿３］，经元素分析、红外光谱表征，并测定了其晶体结构。配合物属正交晶系，Ｐｂｃａ空间群，晶体学参数ａ＝１．４５１５（５），ｂ＝２．２８３３（５），ｃ＝３．３５５４（６）ｎｍ；Ｖ＝１１．１２０９（５）ｎｍ￣３；Ｄ＿ｃ＝１．３１ｇ·ｃｍ￣＿（－３）；Ｆ（０００）＝４４．２３，Ｚ＝８。最后一致性因子Ｒ＝０．０４７，Ｒ＿ｗ＝０．０４５，平均Ｙｂ－Ｎ键长是０．２２６４（９）ｎｍ。

Yb(C_6Me_6)(AlCl_4)_3·MeC_6H_5的合成及其晶体结构

中性芳烃π键金属配合物在成键机制,反应性能方面都有自己的特点,并能催化烯烃聚合,齐聚合或烷基化反应。研究它们的合成,结构和反应性能,无论在理论上还是在实际上都是十分有意义的。近年来,相继报道了 Sm(C_6Me_6)(AlCl_4)_3(1),Ln(C_6H_6)(AlCl_4)_3(2)和Sm(MeC_6H_5)(AlCl_4)_3(3)的合成及结构,但是以上这些配合物都是采用 Friedel—Crafts法合成的。最近我们发现AICI_3,YbC_3,C_6Me_6直接反应可以方便地合成这些配合物。与现用的Friedel—Crafts相比,不仅简化了操作步骤,还提高了产物收率。本文将简要报道这一结果。

CRYSTAL-STRUCTURE OF [YB (NO3)3 (PHEN) (H2O)]CENTER-DOT(12-CROWN-4)

The title complex was prepared by reacting Yb(NO3)3 (12-crown-4) with 1, 10-phenanthiroline (hereafter phen) in acetone. It crystallized in the triclinic space group P1BAR with a = 10.095(5), b = 17.415(4), c = 8.710(2) angstrom; alpha = 92.45(2), beta = 115.83(3), gamma = 74.08(3)degrees and D(c), = 1.85 g cm-3; Z = 2. The metal ion in this complex is nine-coordinated to three bidentate nitrate ions, two nitrogen atoms of a phen and a water molecule. The crown ligand is hydrogen bonded to the coordination water molecule. The symmetry change of the crown ether is also discussed.

EFFECT OF THE CONCENTRATION OF THE ER3+ ION ON THE SPECTRAL INTENSITY PARAMETERS OF ER-YAG CRYSTALS

The absorption spectra of Er:YAG (YAG, yttrium-aluminium-garnet) crystals containing different concentrations of the trivalent erbium ion were measured and the spectral intensity parameters were calculated from these experimental spectra using the Judd-Ofelt model. The results indicate that the phenomenological intensity parameters, OMEGA(lambda) (lambda = 2, 4 and 6), vary as a function of the concentration of the Er3+ ion in the Er:YAG crystal, but no variation in the fluorescence-branching ratios as a function of the concentration of the Er3+ ion is found. An empirical formula is proposed to describe the relationship between the spectral intensity parameters and the Er3+ ion concentration in the Er:YAG crystal. The spectral intensity parameters exhibit a maximum in Er:YAG crystals containing about 1-1.5 at.% Er3+ ion. The effect of the Er3+ ion concentration on the spectral intensity parameters may be attributed to the inhomogeneous lattice distortion in the cell of the Er:YAG crystal caused by the dopant erbium ions.

THE VALENCE CHANGE FROM RE3+ TO RE2+ (RE-EQUIVALENT-TO-EU, SM, YB) IN SRB4O7-RE PREPARED IN AIR AND THE SPECTRAL PROPERTIES OF RE2+

A valence change from RE3+ to RE2+ (RE=Eu, Sm, Yb) was observed in samples of SrB4O7: RE prepared by solid state reaction at high temperature in air. The phosphors SrB4O7: RE2+ show efficient luminescence at room temperature. The broad band d-f emissions of Eu2+ and Yb2+ are at 367 and 360 nm respectively. The sharp line f-f emissions of the Sm2+ ion (5D0-F-7(J)) are in the range 680-780 nm. The probable reasons for the valence change of Eu, Sm and Yb in this host are discussed.

Yb原子奇宇称受扰里德堡系n~1P_1、n~3P_1能级自然辐射寿命的研究

通过激光与原子束相互作用,三步激发及时间分辨光谱术,测量了Yb原子奇宇称受扰里德堡系6snp~(1,3)P_1 21个能级和两个干扰能级的自然辐射寿命,分析了各种因素对测量值的影响.

YAG∶Er~(3+),Ce~(3+)激光晶体的光谱特性

本文采用在YAG晶体中共掺铒铈离子,利用Ce~(3+)离子具有f—d宽带吸收跃迁,提高Er~(3+)离子对泵浦能量的吸收,以降低YAG:Er,Ce晶体的激光阈值。并测定了晶体在室温下的吸收光谱和荧光光谱。讨论了YAG:Er~(3+),Ce~(3+)晶体的光谱特性。用Judd—Ofelt理论计算了晶体中Er~(3+)离子振子强度,并与单掺铒离子YAG:Er~(3+)晶体中的数值进行了比较。

水溶液中甘氨酰替亮氨酸与Ho(ClO_4)_3和Yb(ClO_4)_3相互作用的NMR研究(英文)

本文用~(13)C NMR方法研究了水溶液中三价顺磁性稀土离子Ho~(3+)和Yb~(3+)与二肽甘氨酰替亮氨酸之间的相互作用。对稀土诱导位移中的接触位移和偶极位移进行了分离。实验表明,与羧基相连的碳核所受的接触作用很大,因此不能把镱诱导的位移直接用于肽的构象分析。在水溶液中,肽通过羧基与稀土离子配位,在弱酸性条件下肽键和氨基均不参与配位。根据结构因子确定了肽在溶液中的构象,结果表明,分子片段C1-C2-C5-C6,C2-N-C3-C4和C2-C5-C6-C8为反式,而C2-C5-C6-C7和C1-C2-N-C3成旁式。

YAG:Er~(3+)激光晶体中Er~(3+)红外波段的荧光发射

YAG:Er~(3+)晶体中Er~(3+)在红外新波段所谓“大气窗口”的激光发射,由于具有优异性能,研究此材料者日益增多。但红外波段荧光光谱除有局部的报导外,尚无系统报导,近年来我们对0.80—3.00μm波段的Er~(3+)离子的荧光光谱,进行了较详细的研究,并获得了较为满意的结果。这些结果,对从事YAG:Er~(3+)材料和器件的工作者,无疑是较为有益的参考