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NITROGEN CHEMISORPTION ON THE COORDINATIVELY UNSATURATED RH SITE ON AL2O3

机译:在Al2O3上配位不饱和的RH站点上的氮化学吸附

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The UV (3.8 eV) photolysis of atomically-dispersed Rh-1(CO)(2) species supported on an Al2O3 surface in the presence of N-2 at 175 K caused the replacement of CO by N-2 ligands. Therefore dinitrogen chemisorption effectively probes the coordinatively unsaturated Rh(CO) species generated during photodecomposition of Rh-1(CO)(2)/Al2O3. Two infrared bands, observed at 2234 and 2048 cm(-1), are attributed respectively to nu(N2) and nu(CO) in Rh(N2)(CO), and a band at 2188 cm(-1) is assigned to Rh(N-2)(2) surface species. The assignments are based on frequencies and the relative rates of spectral development for the two N-2-containing species. The Rh(N-2)(2) species on Al2O3 exhibits identical N-N stretching modes to a similar species produced by matrix isolation methods. It is shown that both the Rh-CO bond and the Rh-N-2 bond may be broken by photolysis.
机译:在175 K的N-2存在下,在Al2O3表面上负载的原子分散的Rh-1(CO)(2)物种的UV(3.8 eV)光解导致N-2配体取代了CO。因此,二氮化学吸附有效地探测了Rh-1(CO)(2)/ Al2O3的光分解过程中产生的配位不饱和Rh(CO)物种。在2234和2048 cm(-1)处观察到两个红外波段,分别归因于Rh(N2)(CO)中的nu(N2)和nu(CO),并将2188 cm(-1)处的波段指定为Rh(N-2)(2)表面种类。分配基于两种含N-2物质的频率和光谱发展的相对速率。 Al2O3上的Rh(N-2)(2)物种与通过基质分离方法生产的相似物种具有相同的N-N拉伸模式。结果表明,Rh-CO键和Rh-N-2键都可能被光解而断裂。

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