Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic
Por um escritor misterioso
Last updated 02 setembro 2024
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://pubs.acs.org/cms/10.1021/jacs.2c00305/asset/images/medium/ja2c00305_0015.gif)
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://pubs.acs.org/cms/10.1021/jacs.2c00305/asset/images/large/ja2c00305_0010.jpeg)
Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41557-022-01081-1/MediaObjects/41557_2022_1081_Fig1_HTML.png)
An isolable germylyne radical with a one-coordinate germanium atom
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://www.science.org/cms/10.1126/science.adg2833/asset/15630194-8407-4595-8ae9-6a77ef9ef00f/assets/images/large/science.adg2833-f3.jpg)
Synthesis and isolation of a triplet bismuthinidene with a
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://www.researchgate.net/profile/Alexandra-Slawin/publication/230804497/figure/fig2/AS:281852406452247@1444210258784/Scheme1-Synthesis-and-selected-reactivity-of-the-phosphanylidene-phosphorane-3_Q320.jpg)
Scheme 1. Synthesis and selected reactivity of the phosphanylidene
Trimethylphosphine, C3H9P
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://www.researchgate.net/profile/Gengwen-Tan/publication/319082212/figure/fig2/AS:530336094605315@1503453386042/Frequency-dependence-of-out-of-phase-magnetic-susceptibility-for-1Co-top-and-1Fe.png)
Frequency dependence of out-of-phase ('') magnetic
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0ecbae96-faef-4d11-8895-eaff3744e88b/chem202102320-toc-0001-m.jpg)
Phosphine‐Stabilized Pnictinidenes - Raiser - 2021 - Chemistry
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://onlinelibrary.wiley.com/cms/asset/31188edb-d4bf-49c8-84d1-3b94af47500c/anie202106846-toc-0001-m.jpg)
A Primary Acyl Phosphine Stabilized by a Phosphonium Ylide
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://pubs.acs.org/cms/10.1021/jacs.2c00305/asset/images/medium/ja2c00305_0002.gif)
Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41557-022-01081-1/MediaObjects/41557_2022_1081_Figa_HTML.png)
An isolable germylyne radical with a one-coordinate germanium atom
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://pubs.acs.org/cms/10.1021/jacs.2c00305/asset/images/medium/ja2c00305_0005.gif)
Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](http://junzhu.chem8.org/sites/default/files/anie.202113334.jpg)
Zhu Group at the Chinese University of Hong Kong, Shenzhen
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://pubs.acs.org/cms/10.1021/jacs.2c00305/asset/images/large/ja2c00305_0014.jpeg)
Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41557-022-01081-1/MediaObjects/41557_2022_1081_Fig2_HTML.png)
An isolable germylyne radical with a one-coordinate germanium atom
![Phosphine-Stabilized Germylidenylpnictinidenes as Synthetic](https://www.researchgate.net/publication/230804497/figure/fig2/AS:281852406452247@1444210258784/Scheme1-Synthesis-and-selected-reactivity-of-the-phosphanylidene-phosphorane-3.png)
Scheme 1. Synthesis and selected reactivity of the phosphanylidene
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