hey I know that one
Things I Won't Work With: Azidoazide Azides, More Or Less
www.science.org
October 29, 2026 at 4:25 AM
hey I know that one
www.organic-chemistry.org/abstracts/li...
A copper(I)-catalyzed click/allylation cascade reaction of various alkynes, azides, and allyl bromides provides fully substituted 5-allyl-1,2,3-triazoles.
A copper(I)-catalyzed click/allylation cascade reaction of various alkynes, azides, and allyl bromides provides fully substituted 5-allyl-1,2,3-triazoles.
October 25, 2026 at 6:59 PM
www.organic-chemistry.org/abstracts/li...
A copper(I)-catalyzed click/allylation cascade reaction of various alkynes, azides, and allyl bromides provides fully substituted 5-allyl-1,2,3-triazoles.
A copper(I)-catalyzed click/allylation cascade reaction of various alkynes, azides, and allyl bromides provides fully substituted 5-allyl-1,2,3-triazoles.
www.organic-chemistry.org/abstracts/li...
Transition-metal-free, base-promoted, three-component reactions involving various nitriles, azides, and isothiocyanates provide fully substituted 5-amide-1,2,3-triazole and 5-imide-1,2,3-triazole derivatives.
Transition-metal-free, base-promoted, three-component reactions involving various nitriles, azides, and isothiocyanates provide fully substituted 5-amide-1,2,3-triazole and 5-imide-1,2,3-triazole derivatives.
October 20, 2026 at 12:30 AM
www.organic-chemistry.org/abstracts/li...
Transition-metal-free, base-promoted, three-component reactions involving various nitriles, azides, and isothiocyanates provide fully substituted 5-amide-1,2,3-triazole and 5-imide-1,2,3-triazole derivatives.
Transition-metal-free, base-promoted, three-component reactions involving various nitriles, azides, and isothiocyanates provide fully substituted 5-amide-1,2,3-triazole and 5-imide-1,2,3-triazole derivatives.
Azides?! That's everyones favorite brand!
October 14, 2026 at 10:47 PM
Azides?! That's everyones favorite brand!
THIS IS THE BEST
October 14, 2026 at 6:31 AM
THIS IS THE BEST
Don’t judge me
October 14, 2026 at 8:11 AM
Don’t judge me
🔬 Building complex molecules, one module at a time! Suguru Yoshida & co-workers introduce bis(2-azidoacrylamide)s as versatile tetravalent platforms for the rapid assembly of diverse bis(triazole)s🧩
#ClickChemistry #azides #triazoles
👉 buff.ly/mvH8mlc
#ClickChemistry #azides #triazoles
👉 buff.ly/mvH8mlc
October 14, 2026 at 7:02 AM
🔬 Building complex molecules, one module at a time! Suguru Yoshida & co-workers introduce bis(2-azidoacrylamide)s as versatile tetravalent platforms for the rapid assembly of diverse bis(triazole)s🧩
#ClickChemistry #azides #triazoles
👉 buff.ly/mvH8mlc
#ClickChemistry #azides #triazoles
👉 buff.ly/mvH8mlc
www.organic-chemistry.org/abstracts/li...
A mechanochemical route for a selective synthesis of 4-nitro-1,2,3-triazoles via organocatalyzed oxidative [3 + 2] cycloaddition between β-nitrostyrenes and organic azides
A mechanochemical route for a selective synthesis of 4-nitro-1,2,3-triazoles via organocatalyzed oxidative [3 + 2] cycloaddition between β-nitrostyrenes and organic azides
October 9, 2026 at 5:07 PM
www.organic-chemistry.org/abstracts/li...
A mechanochemical route for a selective synthesis of 4-nitro-1,2,3-triazoles via organocatalyzed oxidative [3 + 2] cycloaddition between β-nitrostyrenes and organic azides
A mechanochemical route for a selective synthesis of 4-nitro-1,2,3-triazoles via organocatalyzed oxidative [3 + 2] cycloaddition between β-nitrostyrenes and organic azides
Nitrogen (N): Triple-Bond Chemistry, Fixation & Energetics
Exhaustive post-graduate masterclass on Nitrogen (Z=7). Covers N2 molecular orbital theory, Haber-Bosch kinetics, biological FeMoco fixation, and azides.
Exhaustive post-graduate masterclass on Nitrogen (Z=7). Covers N2 molecular orbital theory, Haber-Bosch kinetics, biological FeMoco fixation, and azides.
Nitrogen (N): Triple-Bond Chemistry, Fixation & Energetics
Exhaustive post-graduate masterclass on Nitrogen (Z=7). Covers N2 molecular orbital theory, Haber-Bosch kinetics, biological FeMoco fixation, and azides.
thebrokencap.wordpress.com
October 7, 2026 at 5:14 PM
Nitrogen (N): Triple-Bond Chemistry, Fixation & Energetics
Exhaustive post-graduate masterclass on Nitrogen (Z=7). Covers N2 molecular orbital theory, Haber-Bosch kinetics, biological FeMoco fixation, and azides.
Exhaustive post-graduate masterclass on Nitrogen (Z=7). Covers N2 molecular orbital theory, Haber-Bosch kinetics, biological FeMoco fixation, and azides.
This year's #NobelPrize in Chemistry will be awarded tomorrow 🏅
Here's a reminder of the research that has won in previous years, including molecular sponges, the prediction of protein structures, and clicking together new medicine molecules: www.compoundchem.com/category/nob...
#ChemSky 🧪
Here's a reminder of the research that has won in previous years, including molecular sponges, the prediction of protein structures, and clicking together new medicine molecules: www.compoundchem.com/category/nob...
#ChemSky 🧪
October 6, 2026 at 5:30 PM
This year's #NobelPrize in Chemistry will be awarded tomorrow 🏅
Here's a reminder of the research that has won in previous years, including molecular sponges, the prediction of protein structures, and clicking together new medicine molecules: www.compoundchem.com/category/nob...
#ChemSky 🧪
Here's a reminder of the research that has won in previous years, including molecular sponges, the prediction of protein structures, and clicking together new medicine molecules: www.compoundchem.com/category/nob...
#ChemSky 🧪
Hiroyuki Morimoto & co-workers investigate functional group tolerance in #CuAAC using a functional group evaluation kit🧪 The study highlights the importance of ligand selection and shows how switching to SPAAC can overcome thiol-induced reactivity issues⚡
#azides #triazoles
👉 buff.ly/hzkQLNK
#azides #triazoles
👉 buff.ly/hzkQLNK
September 30, 2026 at 7:01 AM
Hiroyuki Morimoto & co-workers investigate functional group tolerance in #CuAAC using a functional group evaluation kit🧪 The study highlights the importance of ligand selection and shows how switching to SPAAC can overcome thiol-induced reactivity issues⚡
#azides #triazoles
👉 buff.ly/hzkQLNK
#azides #triazoles
👉 buff.ly/hzkQLNK
Embracing triplet nitrenes for C-to-N replacement of complex bicyclic (hetero)aryl azides
Checking your browser - reCAPTCHA
ift.tt
September 28, 2026 at 7:35 AM
Embracing triplet nitrenes for C-to-N replacement of complex bicyclic (hetero)aryl azides
September 24, 2026 at 6:04 PM
oh no I read the dimethyl mercury stuff. the "what if we fill a solid rocket booster with heavy metal azides" work is hair-raising too.
September 19, 2026 at 12:41 AM
oh no I read the dimethyl mercury stuff. the "what if we fill a solid rocket booster with heavy metal azides" work is hair-raising too.
🔔 Research article by Motoki Ito, Shigeo Sugiyama 𝘦𝘵 𝘢𝘭.
Protonation-assisted regioselectivity control in cycloaddition of (iso)quinolynes and azides
🔗 doi.org/10.1039/d6qo...
#Cycloaddition #Azides #Regioselectivity #Arynes #Heterocycles
Protonation-assisted regioselectivity control in cycloaddition of (iso)quinolynes and azides
🔗 doi.org/10.1039/d6qo...
#Cycloaddition #Azides #Regioselectivity #Arynes #Heterocycles
September 9, 2026 at 3:46 AM
🔔 Research article by Motoki Ito, Shigeo Sugiyama 𝘦𝘵 𝘢𝘭.
Protonation-assisted regioselectivity control in cycloaddition of (iso)quinolynes and azides
🔗 doi.org/10.1039/d6qo...
#Cycloaddition #Azides #Regioselectivity #Arynes #Heterocycles
Protonation-assisted regioselectivity control in cycloaddition of (iso)quinolynes and azides
🔗 doi.org/10.1039/d6qo...
#Cycloaddition #Azides #Regioselectivity #Arynes #Heterocycles
@cjust bonus points for “electronegative hate”. I lol’d.
That said: check out fluorine.
And if the writing makes you smile, my favorite page-long essay of similar ‘but why would you’ https://www.science.org/content/blog-post/things-i-won-t-work-azidoazide-azides-more-or-less
That said: check out fluorine.
And if the writing makes you smile, my favorite page-long essay of similar ‘but why would you’ https://www.science.org/content/blog-post/things-i-won-t-work-azidoazide-azides-more-or-less
August 31, 2026 at 7:55 PM
@cjust bonus points for “electronegative hate”. I lol’d.
That said: check out fluorine.
And if the writing makes you smile, my favorite page-long essay of similar ‘but why would you’ https://www.science.org/content/blog-post/things-i-won-t-work-azidoazide-azides-more-or-less
That said: check out fluorine.
And if the writing makes you smile, my favorite page-long essay of similar ‘but why would you’ https://www.science.org/content/blog-post/things-i-won-t-work-azidoazide-azides-more-or-less
www.organic-chemistry.org/abstracts/li...
A regio- and stereoselective thermal cycloaddition of azides to acetoxy allenoates as 1,2-dipoles provides 1,4,5-tri/1,5-disubstituted 1,2,3-triazoles
A regio- and stereoselective thermal cycloaddition of azides to acetoxy allenoates as 1,2-dipoles provides 1,4,5-tri/1,5-disubstituted 1,2,3-triazoles
August 25, 2026 at 4:14 PM
www.organic-chemistry.org/abstracts/li...
A regio- and stereoselective thermal cycloaddition of azides to acetoxy allenoates as 1,2-dipoles provides 1,4,5-tri/1,5-disubstituted 1,2,3-triazoles
A regio- and stereoselective thermal cycloaddition of azides to acetoxy allenoates as 1,2-dipoles provides 1,4,5-tri/1,5-disubstituted 1,2,3-triazoles
www.organic-chemistry.org/abstracts/li...
A Fe(III)-based metalloradical catalysis system enables an efficient asymmetric C–H amination for an enantioselective synthesis of chiral indolines from aryl azides.
A Fe(III)-based metalloradical catalysis system enables an efficient asymmetric C–H amination for an enantioselective synthesis of chiral indolines from aryl azides.
August 22, 2026 at 9:00 AM
www.organic-chemistry.org/abstracts/li...
A Fe(III)-based metalloradical catalysis system enables an efficient asymmetric C–H amination for an enantioselective synthesis of chiral indolines from aryl azides.
A Fe(III)-based metalloradical catalysis system enables an efficient asymmetric C–H amination for an enantioselective synthesis of chiral indolines from aryl azides.
And some theory on bulky singlet Arylnitrene.
Impact of Bulky Substituents on the Singlet Arylnitrene Ring Enlargement
Substituents of the hydrindacene type allow the isolation of crystalline stable triplet arylnitrenes from photodecomposition of the corresponding aryl azides, while phenyl azide is known to produce si...
pubs.acs.org
November 8, 2025 at 9:03 PM
And some theory on bulky singlet Arylnitrene.
“I love the smell of azides in the morning!”
a man stands in front of a blackboard with the word example on it
ALT: a man stands in front of a blackboard with the word example on it
media.tenor.com
August 24, 2025 at 1:43 AM
“I love the smell of azides in the morning!”
So, you’re into adventure…
Maybe you’ve:
Climbed Everest
Went diving with sharks
Wore a red shirt on Star Trek
Heated azides in a sealed vial
But you’ve never lived until you’ve used a weed trimmer alongside a pea gravel pathway…
While wearing shorts and sandals
Maybe you’ve:
Climbed Everest
Went diving with sharks
Wore a red shirt on Star Trek
Heated azides in a sealed vial
But you’ve never lived until you’ve used a weed trimmer alongside a pea gravel pathway…
While wearing shorts and sandals
a man in a blue suit and tie is laughing with the words knights of columbus that hurt
ALT: a man in a blue suit and tie is laughing with the words knights of columbus that hurt
media.tenor.com
July 15, 2025 at 11:58 PM
So, you’re into adventure…
Maybe you’ve:
Climbed Everest
Went diving with sharks
Wore a red shirt on Star Trek
Heated azides in a sealed vial
But you’ve never lived until you’ve used a weed trimmer alongside a pea gravel pathway…
While wearing shorts and sandals
Maybe you’ve:
Climbed Everest
Went diving with sharks
Wore a red shirt on Star Trek
Heated azides in a sealed vial
But you’ve never lived until you’ve used a weed trimmer alongside a pea gravel pathway…
While wearing shorts and sandals
A Cluster publication by 1st author Young Scientist Julian Brückel presents a series of aromatic, polyazide-containing building blocks that enable the formation of a new class of amorphous #porous #organic #materials! https://doi.org/10.1002/cnma.202300222 #azides #ATFs @braeselab...
March 11, 2025 at 6:10 PM
A Cluster publication by 1st author Young Scientist Julian Brückel presents a series of aromatic, polyazide-containing building blocks that enable the formation of a new class of amorphous #porous #organic #materials! https://doi.org/10.1002/cnma.202300222 #azides #ATFs @braeselab...
Metal-Organic Framework Thin Films as Ideal Matrices for Azide Photolysis in Vacuum: New Cluster publication with @StefanBraese reports the in situ spectroscopic observation of UV-induced photochemical reactions of aryl azides within a crystalline matrix....
March 11, 2025 at 5:06 PM
Metal-Organic Framework Thin Films as Ideal Matrices for Azide Photolysis in Vacuum: New Cluster publication with @StefanBraese reports the in situ spectroscopic observation of UV-induced photochemical reactions of aryl azides within a crystalline matrix....
Holy moley! Careful oxidation of an azide at very low temps gives rise to an absolutely bonkers bonkers bonkers molecule: N6!!
An allotrope of nitrogen! And it seems to be stable at liquid nitrogen temperature, 77 K. Look at the isotopic signature in the […]
[Original post on mastodon.social]
An allotrope of nitrogen! And it seems to be stable at liquid nitrogen temperature, 77 K. Look at the isotopic signature in the […]
[Original post on mastodon.social]
June 18, 2025 at 8:10 PM
Holy moley! Careful oxidation of an azide at very low temps gives rise to an absolutely bonkers bonkers bonkers molecule: N6!!
An allotrope of nitrogen! And it seems to be stable at liquid nitrogen temperature, 77 K. Look at the isotopic signature in the […]
[Original post on mastodon.social]
An allotrope of nitrogen! And it seems to be stable at liquid nitrogen temperature, 77 K. Look at the isotopic signature in the […]
[Original post on mastodon.social]