Baljozović Miloš, Pijeat Joffrey, Campidelli Stéphane, Ernst Karl-Heinz
Molecular Surface Science Group, Empa, 8600 Dübendorf, Switzerland.
Université Paris-Saclay, CEA, CNRS, NIMBE, LICSEN, 91191 Gif-sur-Yvette, France.
J Am Chem Soc. 2024 Dec 18;146(50):34600-34608. doi: 10.1021/jacs.4c12460. Epub 2024 Dec 4.
Recent advancements in on-surface synthesis have enabled the reliable and predictable preparation of atomically precise low-dimensional materials with remarkable properties, which are often unattainable through traditional wet chemistry. Among these materials, porphyrins stand out as a particularly intriguing class of molecules, extensively studied both in solution and on surfaces. Their appeal lies in the ability to fine-tune their unique chemical and physical properties through central metal exchange or peripheral functionalization. However, the synthesis of π-extended porphyrins featuring unsubstituted anthracenyl groups has remained elusive. Herein, we report an temperature-controlled cyclodehydrogenation of bis- and tetraanthracenyl Zn(II) porphyrins on a gold(111) surface. By gradually increasing the temperature, sequential dehydrogenation leads to the formation of fused anthracenyl porphyrin products. Notably, at high molecular coverage, the formation of bowl-shaped porphyrins occurs, along with transmetalation of Zn with Au. These findings open the door to a variety of π-extended anthracenyl-containing porphyrin products via cyclodehydrogenation and transmetalation, offering significant potential in the fields of molecular (photo/electro)catalysis, (opto)electronics, and spintronics.
表面合成领域的最新进展使得人们能够可靠且可预测地制备出具有卓越性能的原子精确低维材料,而这些性能通常是传统湿化学方法无法实现的。在这些材料中,卟啉作为一类特别引人关注的分子脱颖而出,在溶液和表面都得到了广泛研究。它们的吸引力在于能够通过中心金属交换或外围功能化来微调其独特的化学和物理性质。然而,具有未取代蒽基的π-扩展卟啉的合成仍然难以实现。在此,我们报道了双蒽基和四蒽基锌(II)卟啉在金(111)表面的温控环脱氢反应。通过逐渐升高温度,连续脱氢导致稠合蒽基卟啉产物的形成。值得注意的是,在高分子覆盖率下,会形成碗状卟啉,同时锌与金发生金属转移。这些发现为通过环脱氢和金属转移制备各种π-扩展含蒽基卟啉产物打开了大门,在分子(光/电)催化、(光)电子学和自旋电子学领域具有巨大潜力。