Zhang Boyi (@zhangboyi9) 's Twitter Profile
Zhang Boyi

@zhangboyi9

PhD candidate in Prof. Wu Jishan's group🇸🇬

ID: 1354602260370575362

calendar_today28-01-2021 01:28:50

58 Tweet

89 Followers

74 Following

Jishan Wu (@jishan_wu) 's Twitter Profile Photo

This piece of work is now officially published in Nature Synthesis. Thank all reviewers for their constructive comments! nature.com/articles/s4416…

Jishan Wu (@jishan_wu) 's Twitter Profile Photo

Aromaticity in 2D fully conjugated multicyclic macrocycles! We demonstrate nearly "one-pot" synthesis and show how the macrocycles interplay with each other at different redox states. Paper was just published in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

Aromaticity in 2D fully conjugated multicyclic macrocycles! We demonstrate nearly "one-pot" synthesis and show how the macrocycles interplay with each other at different redox states. Paper was just published in <a href="/J_A_C_S/">J. Am. Chem. Soc.</a>
pubs.acs.org/doi/10.1021/ja…
Qing-Hui Guo (郭庆辉) (@huiguo8) 's Twitter Profile Photo

Delighted and excited to share the first publication from my group at Zhejiang University out in J. Am. Chem. Soc.! We report the topochemical synthesis of soluble and processable polymeric single crystals with rigid polycationic backbones. Many thanks to Fraser Stoddart bit.ly/3J807pI

Jishan Wu (@jishan_wu) 's Twitter Profile Photo

Radical-radical coupling and radical-mediated coupling approaches toward monolayer and bilayer graphene fragments! We also observed an unusual 32-center-2-electron covalent π-bonding. Paper was just published in Nature Synthesis. Tianyu Jiao SunZhe nature.com/articles/s4416…

Radical-radical coupling and radical-mediated coupling approaches toward monolayer and bilayer graphene fragments! We also observed an unusual 32-center-2-electron covalent π-bonding. Paper was just published in <a href="/NatureSynthesis/">Nature Synthesis</a>. <a href="/TianyuJiao223/">Tianyu Jiao</a> <a href="/zhesuntju/">SunZhe</a>
nature.com/articles/s4416…
Jishan Wu (@jishan_wu) 's Twitter Profile Photo

Extended zethrenes showing a stable helical structure with an end-to-end twist of up to 201 dgree! Paper was just published in Chemical Science as part of the special issue to celebrate the 130th anniversary of Wuhan University. Sun Zhitao SunZhe pubs.rsc.org/en/content/art…

Extended zethrenes showing a stable helical structure with an end-to-end twist of up to 201 dgree! Paper was just published in <a href="/ChemicalScience/">Chemical Science</a> as part of the special issue to celebrate the 130th anniversary of Wuhan University. <a href="/sunzhitao1998/">Sun Zhitao</a> <a href="/zhesuntju/">SunZhe</a> pubs.rsc.org/en/content/art…
Chunyan Chi (@cchigroup) 's Twitter Profile Photo

Circumpentacene has been synthesized and exhibits open-shell diradical charater, good stability, and amphoteric redox behavior. Find out more in our new Angewandte Chemie research article onlinelibrary.wiley.com/doi/10.1002/an… Congrats to Qing, Haipeng and Xudong Hou. NUS Chemistry @ResearchFos

Circumpentacene has been synthesized and exhibits open-shell diradical charater, good stability, and amphoteric redox behavior. Find out more in our new <a href="/angew_chem/">Angewandte Chemie</a> research article onlinelibrary.wiley.com/doi/10.1002/an…
Congrats to Qing, Haipeng and <a href="/David81601788/">Xudong Hou</a>. <a href="/ChemNUS/">NUS Chemistry</a> @ResearchFos
Aurelio Mateo-Alonso (@kokelab) 's Twitter Profile Photo

Just out in Chem! An accelerated iterative synthesis of ultralong molecular GNRs! The longest displays a 920-atoms core with a 36-nm long (147 linearly fused rings) backbone. 👉tinyurl.com/2wef82ke Don’t forget to sing the #JurassicPark theme while watching the video 🦕

Leo Gross (@leo_gross_ibm) 's Twitter Profile Photo

Together with Harry Anderson Group we made an antiaromatic carbon allotrope. It is a molecule called cyclo[16]carbon. And it even is doubly-antiaromatic. What that means and how that was done, you can read in Nature: nature.com/articles/s4158…

Jishan Wu (@jishan_wu) 's Twitter Profile Photo

A core expanded [10]annulene! We observed co-existence of Möbius/Hückel topology and aromaticity/antiaromaticity in its dication, presumably due to the balance between strain and aromaticity. Paper was just published Angewandte Chemie : onlinelibrary.wiley.com/doi/10.1002/an…

A core expanded [10]annulene! We observed co-existence of Möbius/Hückel topology and aromaticity/antiaromaticity in its dication, presumably due to the balance between strain and aromaticity. Paper was just published <a href="/angew_chem/">Angewandte Chemie</a> : onlinelibrary.wiley.com/doi/10.1002/an…
Jishan Wu (@jishan_wu) 's Twitter Profile Photo

A molecular "X" made by chemists, free for Elon Musk !😀 It is a topologically frustrated and strongly correlated tetraradical system. This collaborative work is now in Nature Chemistry

A molecular "X" made by chemists, free for <a href="/elonmusk/">Elon Musk</a> !😀 It is a topologically frustrated and strongly correlated tetraradical system. This collaborative work is now in <a href="/NatureChemistry/">Nature Chemistry</a>
SunZhe (@zhesuntju) 's Twitter Profile Photo

Excited to share our recent discovery on a two-stage ring cyclization to circumchrysene from a doubly helical diradicaloid! Many thanks to the reviewers for the very detailed and insightful suggestions!

Leo Gross (@leo_gross_ibm) 's Twitter Profile Photo

Cyclocarbon C18 (doubly aromatic) is a freak, C16 (doubly anti-aromatic) a superfreak, C13 is the freakiest of them all: triplet ground state, more or less delocalized carbene center, and neither Baird's nor Hueckel's rule can be applied. science.org/doi/10.1126/sc…

Cyclocarbon C18 (doubly aromatic) is a freak, C16 (doubly anti-aromatic) a superfreak, C13 is the freakiest of them all: triplet ground state, more or less delocalized carbene center, and neither Baird's nor Hueckel's rule can be applied. science.org/doi/10.1126/sc…
ChemistryViews (@chemistryviews) 's Twitter Profile Photo

Aza-Superbenzene and Aza-Supernaphthalene: Dications, tetracations, and hexacations of a tetraazasuperbenzene and a hexaazasupernaphthalene show global aromaticity or anti-aromaticity (work published in Angewandte Chemie) chemistryviews.org/aza-superbenze…

Aza-Superbenzene and Aza-Supernaphthalene:
Dications, tetracations, and hexacations of a tetraazasuperbenzene and a hexaazasupernaphthalene show global aromaticity or anti-aromaticity
(work published in <a href="/angew_chem/">Angewandte Chemie</a>)
chemistryviews.org/aza-superbenze…
Jishan Wu (@jishan_wu) 's Twitter Profile Photo

A rhombus-shaped hydrocarbon, [4]rhombene, was synthesized and applied for organic lasers with emission beyond 830 nm. This collaborative work with Maria's team is now published in Angewandte Chemie. Congratulations to Shen Tong and other co-authors! onlinelibrary.wiley.com/doi/10.1002/an…

A rhombus-shaped hydrocarbon, [4]rhombene, was synthesized and applied for organic lasers with emission beyond 830 nm. This collaborative work with Maria's team is now published in <a href="/angew_chem/">Angewandte Chemie</a>. Congratulations to <a href="/ShenTon44744598/">Shen Tong</a> and other co-authors! onlinelibrary.wiley.com/doi/10.1002/an…