SPMLabJUK

Our recent manuscript nature.com/articles/s4146… with @icmm_csic @EsisnaI @depena33 @ciqususc espeem.com selected in Editors’ Highlights webpage of research called "Materials science and chemistry” in @NatureComms nature.com/articles/s4146… nature.com/collections/ee…

Excited to share that the acene family has grown with its longest member yet, pentadecacene (15ac), which we synthesized and characterized on a gold surface. @BettingerLab @RalfTonner. Congrats to Zilin, Jakob, John, Tim, Laurentia, Felix! @ERC_Research @SFB1083 @ProLOEWE.

Happy to see our new manuscript on substrate independent planarization yielding nanographenes published in @NatureComms Great collaboration with our friends from @icmm_csic , @EsisnaI , @depena33 , @ciqususc , espeem.com

I love this reaction: atomic hydrogen as catalyst in cyclodehydrogenation reactions. It sounds counterintuitive but it works! Great collaboration with our friends in Krakow @SPMLabJUK , espeem.com and Madrid @EsisnaI @ciqususc @NatureComms

If your reserch relates to on-surface synthesis, don´t miss your chance to submit your abstract to #OSS24 (oss24.dipc.org) before the extended deadline: Marth 14th. Hope to see you in San Feliu de Guixols!

What a way to end the week⚡️Today our work in @angew_chem exploring the on-surface synthesis of NGs embedding azulene and Stone-Wales units is out🎉 @nacho_urgel @XinliangF @davidecijalab @FZU_AVCR @IMDEA_Nano Read more⬇️ onlinelibrary.wiley.com/doi/10.1002/an…

On-Surface Synthesis and Determination of the Open-Shell Singlet Ground State of Tridecacene (Szymon Godlewski and co-workers) @SPMLabJUK, @nanosurflab, @Echavarren_Lab onlinelibrary.wiley.com/doi/10.1002/an…

Dont forget to also check out this work on tridecacene molecule from @GottfriedGroup @RalfTonner @BettingerLab pubs.acs.org/doi/10.1021/ja…

In our last work published in @angew_chem we unveil the open-shell structure of tridecacene and its spin excitation with state-of-the-art quantum chemistry calculations👨‍💻 In collaboration with @SPMLabJUK @Echavarren_Lab onlinelibrary.wiley.com/doi/abs/10.100…

Interested in the latest Communications? Read 'On surface synthesis of an eleven-ring sulfur-doped nonacene' by Antonio Echavarren, Szymon Godlewski, Mariusz Krawiec and first author Irena Padniuk @Echavarren_Lab pubs.rsc.org/en/content/art… pubs.rsc.org/en/content/art…

Organic synthesis, electron microscopy, and computer modeling go hand in hand to uncover the chemical reactions behind nanographenes with pentagonal rings. @ManuelMelleLab @SPMLabJUK @depena33 @ciceco_ua @ciqususc go.acs.org/7vx

Some alkenes are just made different 🦄. The story of tetrafluorenofulvalene, a sterically frustrated oligoradicaloid, now in @NatureChemistry . Congratulations to @ambhore_madan and Bibek Prajapati 😃 doi.org/10.1038/s41557…

On-surface synthesis of graphene nanostructures on TiO2: expanding the range of substrates to obtain well-defined nanographenes by bottom-up approaches. 🆕 #CiQUS collab with @SPMLabJUK just out in @acsnano👇 pubs.acs.org/doi/10.1021/ac… @depena33 @DoloresPMeiras #FEDERGalicia

our new article in @acsnano about efficient on-surface synthesis of nanographene and GNRs on semiconducting TiO2 surface. in collab with @ciqususc @depena33 lab and espeem.com. check it: pubs.acs.org/doi/10.1021/ac…

Porous nanographene C108: detailed electronic structure by advanced STS techniques. Glad to see this out in @CommsMaterials and to be part of this great collaboration within @SFB1083 !

Adsorption Behavior of 9-Anthracenecarboxylic Acid on (110) Rutile TiO2 pubs.acs.org/doi/10.1021/ac…

New review in @JPolymSci: On‐surface synthesis and atomic scale characterization of unprotected indenofluorene polymers by Marco Di Giovannantonio and @FaselRoman. @snsf_ch @NanotechSurfLab onlinelibrary.wiley.com/doi/10.1002/po… #OpenAccess

!!!!!! PLEASE RT WIDELY !!!!!! 1/2 Ukrainian scientists who left Ukraine due to war or plan to leave in the coming days; we will help find accommodation and jobs. Contact us here: mail.amu.pan@gmail.com

We synthesized three nitrogen-substituted undecacenes! The one with aza groups shows considerable radical character and the ones with hydro-aza groups show anti-aromaticity. Check it out at nature.com/articles/s4146…

Don't miss our @Echavarren_Lab last work published in @ChemCommun "On-surface synthesis of a phenylene analogue of nonacene" in collaboration with @JagiellonskiUni @UMCSLublin and @WCh_UWr 🙂👏⚗️🧪🥽👩‍🔬📔👨‍🔬 Otilia Stoica @BlieckRemi @ICIQchem pubs.rsc.org/en/Content/Art…