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内蒙古大学, 化学化工学院,内蒙古 呼和浩特,010021
纸质出版日期:2008-9-20,
收稿日期:2007-11-10,
修回日期:2008-1-15,
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石晓燕, 李文先, 秦彩花, 郭磊, 孙晓军, 孙雪莲, 耿刚强. 二苯基亚砜、苯甲酸与轻稀土高氯酸四元配合物的合成表征及光致发光[J]. 发光学报, 2008,29(5): 772-778
SHI Xiao-yan, LI Wen-xian, QIN Cai-hua, GUO Lei, SUN Xiao-jun, SUN Xue-lian, GENG Gang-qian. Synthesis and Characterization of Quaternary Complexes of Light Rare Earth Perchlorate with Diphenyl Sulfoxide,Benzoic Acid and Studies on Fluorescence of Eu<sup>3+</sup> Complex[J]. Chinese Journal of Luminescence, 2008,29(5): 772-778
石晓燕, 李文先, 秦彩花, 郭磊, 孙晓军, 孙雪莲, 耿刚强. 二苯基亚砜、苯甲酸与轻稀土高氯酸四元配合物的合成表征及光致发光[J]. 发光学报, 2008,29(5): 772-778 DOI:
SHI Xiao-yan, LI Wen-xian, QIN Cai-hua, GUO Lei, SUN Xiao-jun, SUN Xue-lian, GENG Gang-qian. Synthesis and Characterization of Quaternary Complexes of Light Rare Earth Perchlorate with Diphenyl Sulfoxide,Benzoic Acid and Studies on Fluorescence of Eu<sup>3+</sup> Complex[J]. Chinese Journal of Luminescence, 2008,29(5): 772-778 DOI:
合成并表征了高氯酸稀土与二苯基亚砜、苯甲酸的四种四元配合物.经元素分析、稀土络合滴定、摩尔电导率及差热-热重分析
表明四元配合物组成为[
REL
5
L
'(ClO
4
)](ClO
4
)(
RE
=La
Pr
Nd
Eu;
L
=C
6
H
5
SOC
6
H
5
L
'=C
6
H
5
COO
-
).在红外光谱中
第一配体二苯基亚砜的ν
S-O
的特征吸收峰出现在1037cm
-1
处
而各稀土配合物的ν
S-O
向低波数移动到984~989cm
-1
红移50cm
-1
左右
表明稀土离子与亚砜基团的氧原子之间发生配位作用.第二配体苯甲酸钠的反对称伸缩振动吸收峰ν
as(COO
-
)
出现在1550cm
-1
对称伸缩振动吸收峰ν
s(COO
-
)
出现在1416cm
-1
处
羧基伸缩振动吸收频率差Δn[ν
as(COO
-
)
-ν
s(COO
-
)
]值为134cm
-1
;在所有配合物的红外光谱图中ν
as(COO
-
)
向高波数方向发生了位移
而ν
s(COO
-
)
向低波数方向发生了位移
并且Δ
n
值均大于钠盐的Δ
n
值
由此可以认为配合物中羧基是通过单齿方式与稀土离子配位.测定了配合物在丙酮溶液中的摩尔电导率
根据配合物在常见有机溶剂中的摩尔电导率与正负离子的关系结合配合物的红外光谱中高氯酸根离子的四条特征吸收带
表明配合物为1:1型电解质
两个ClO
4
-
无机抗衡阴离子
其中一个在外界
一个进入内界与稀土离子配位.配合物的荧光发射光谱表明
四元配合物的荧光强度比二苯基亚砜高氯酸稀土二元配合物的荧光强度提高469%.磷光光谱表明苯甲酸三重态能级的下限和二苯亚砜三重态能级的上限重叠
导致三重态能级范围扩大
由此可见第二配体的加入提高了配体的三重态能级与Eu
3+
离子
5
D
0
能级的匹配程度.同时在配合物的荧光发射光谱中还可以看到铕离子的电偶极跃迁强度大于磁偶极跃迁
表明稀土离子不处于晶体场的对称中心.在四元配合物中
由于第二配体的加入
往往会降低配合物的对称性
从而增强稀土离子的荧光强度.本文合成的稀土配合物具有良好的荧光性能
而且在室温下稳定
溶解性好
分解温度较高.
Four solid quaternary complexes of light rare earth perchlorate with diphenyl sulfoxide (
L
) and benzoic acid (
L
') have been synthesized and characterized.By elemental analysis
TGA-DTAand themolar conductivities in acetone solution studies
the composition of the complexeswere suggested as [
REL
5
L
'(ClO
4
)](ClO
4
) (
RE
=La
Pr
Nd
Eu;
L
=C
6
H
5
SOC
6
H
5
L
'=C
6
H
5
COO
-
).As shown in IRspectra
the absorption band associated with the S-Ostretching modes in the first ligand diphenyl sulfoxide appears at 1037 cm
-1
while the absorption bands in the complexes appear between 987 cm
-1
and 989 cm
-1
.Ashift of the S-Ostretching frequency towards lowerwave number by about 50 cm
-1
suggests that rare earth ions are bonded with an oxygen atom in sulfoxyl group.In the second ligand benzoate
the absorption band associated with ν
as(COO
-
)
appears at 1550 cm
-1
ν
s(COO
-
)
appears at 1416 cm
-1
.The value of Δn[ν
as(COO
-
)
-ν
s(COO
-
)
] is 134 cm
-1
.Ashift of ν
as(COO
-
)
frequency in complexes towards higherwave number
while a shift of ν
s(COO
-
)
frequency in complexes towards lower wave number.What's more
the value of Δn[ν
as(COO
-
)
-ν
s(COO
-
)
] in complexes is higher than that of Δn[ν
as(COO
-
)
-ν
s(COO
-
)
] in sodium benzoate.This showed that benzoate (
L
') bonded with
RE
3+
ions by one oxygen atom in carboxylgroupwhich coordinate as an unidentate group.One of two perchlorates (ClO
4
-
) is coordinated with
RE
3+
while another is not.Fluorescent spectra of Eu
3+
complex showed thatquaternary complexes have stronger fluorescence than the binary one whose ligand is diphenyl sulfoxide
(the fluorescence intensity of Eu
3+
complex increased by 469%).Phosphorescent spectra of two ligands showed that the lower limit of the triplet state with benzoic acid was overlapped by the upper limit with diphenyl sulfoxide
the energy level range of triplet state was extended.As a result
matching extent of triplet state of ligandswith excited state of the rare earths have been increased by coordination of the second ligand benzoic acid
the transmit efficiency also have been increased.Attributed to the addition of the second ligand
the symmetry of the complexes always have been decreased
as a result
the fluorescence intensitywas increased.
二苯基亚砜苯甲酸轻稀土四元配合物磷光光谱发光
light rare earth quaternary complexesdiphenyl sulfoxidebenzoic acidfluorescencephosphorescent spectr
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