求化学翻译Heterospin systems have received intense interest in the fieldof molecular magnetism.1 Such systems represent oneparticularly promising strategy for the design of molecularmagnetic materials such as high TC molecular-based magnets,2mul

求化学翻译Heterospin systems have received intense interest in the fieldof molecular magnetism.1 Such systems represent oneparticularly promising strategy for the design of molecularmagnetic materials such as high TC molecular-based magnets,2mul
求化学翻译
Heterospin systems have received intense interest in the field
of molecular magnetism.1 Such systems represent one
particularly promising strategy for the design of molecular
magnetic materials such as high TC molecular-based magnets,2
multifunctional materials,3 and single-chain magnets.4 Most
reported heterospin systems so far are constructed from two
different spin carriers such as 3d−3d′,5 3d−4d,6 3d−4f,7 2p−3d,8
and 2p−4f.9 In contrast, very few heterospin compounds
containing three different spin carriers have been obtained
owing to the synthetic challenges inherent in their creation,10 and
only two examples with three different types of spin carriers, 2p−
3d−4f11 and 3p−3d−4f,12 were reported recently. On the other
hand, nitronyl nitroxide radicals can directly bind metal ions not
only to generate heterospin compounds but also to produce the
strongest possible magnetic coupling. Most of nitronyl nitroxide
metal compounds reported to date are based on 3d or 4f metal
ions having zero- and one-dimensional (1D) structure,8a,9 while
the nitronyl nitroxide radical bridged 3d−4f complexes have not
been reported. According to the soft−hard principle, the
lanthanide ions are hard acids; thus, they prefer O rather than
N donor atoms, while 3d metal ions, as borderline acids, have a
strong affinity with N and O donor atoms.13 Thus, in order to
combine 3d and 4f ions within one system, we use a 2-[4-(5-
pyrimidyl)phenyl]-4,4,5,5-tetramethylimidazoline-1-oxyl-3-
oxide (NITPhPyrim) radical ligand containing N and O donor
atoms to build 3d−4f complexes. Noticeably, 3d-rad or 4f-rad
complexes have been obtained by using nitronyl ntroxide radicals
with N donor atoms.14 In this communication, we report on the
synthesis, crystal structure, and magnetic properties of two novel
two-dimensional (2D) compounds, {Ln(hfac)3[Cu-
(hfac)2]3(NITPhPyrim)2} [Ln = Gd (1), Dy (2); hfac =
hexafluoroacetylacetonate], which contain three different types
of spin carriers: a nitronyl nitroxide radical (2p), a 3d metal ion
(Cu2+), and a rare earth ion, 4f (Gd3+or Dy3+). To our
knowledge, they are the first reported 2D 2p−3d−4f compounds
in which a nitronyl nitroxide radical acts as a bridging ligand.

求化学翻译Heterospin systems have received intense interest in the fieldof molecular magnetism.1 Such systems represent oneparticularly promising strategy for the design of molecularmagnetic materials such as high TC molecular-based magnets,2mul
异自旋系统得到了在该领域的强烈兴趣
分子磁性.1个这样的系统代表了一个
特别是有前途的分子设计策略
磁性材料如高胆固醇分子基磁体,2
多功能材料,3和单链磁体4大部分
报道到目前为止异自旋系统由两个
不同的自旋载体如三维−三维′,5三维−4D,4F 6三维−,7 2p−3D,8
−和2P 4F.9相反,很少异自旋化合物
包含三个不同的自旋运营商已经获得
由于在创作中所固有的合成挑战,10
只有两个例子的自旋载流子的三种不同的类型,2P−
三维−4F11和3P−三维−4F,12例报道.另
一方面,氮氧自由基可以直接结合的金属离子不
只有产生异自旋化合物也产生
最可能的磁耦合.大部分的氮氧自由基
金属化合物的报告的日期是基于3d或4f金属
具有零和一维（1D）离子结构,8,9
的氮氧自由基桥联配合物没有3D−4F
被报道.根据软−硬的原则
镧系离子硬酸；因此,他们更喜欢啊,而不是
N供体原子,而三维金属离子,如边缘性酸,有
较强的亲和力与N和O供体atoms.13因此,为了
结合3d和4f离子在一个系统中,我们使用一个2 - [ 4（5—
嘧啶基）苯基] - 4,4,5,5-tetramethylimidazoline-1-oxyl-3—
氧化物（nitphpyrim）基配体的含氮、氧供
原子建立三维−4f配合物.值得注意的是,3D RAD或4f拉德
配合物进行了氮ntroxide基得到的
在这种沟通atoms.14供氮,我们报告
的合成,晶体结构,和两个新的磁特性
二维（2D）化合物,{ LN 3 [铜（HFAC）—
（HFAC）2 ] 3（nitphpyrim）2 } [ Ln = Gd,Dy（1）（2）；HFAC =
六氟乙酰丙酮],其中包含三种不同的类型
自旋载体：一个氮氧自由基（2p）,一个三维的金属离子
（Cu2 +的）,和稀土离子的4f（Gd3 +,或Dy3 +）.我们的
知识,他们是第一个报道二维2P−三维−4f化合物
其中的氮氧自由基作为桥联配体.
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