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![The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/2807c00e-944a-4528-b881-a84c309ddda3/mfig008.jpg "The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library")
The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library
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![The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/71451462-7578-4e39-90b0-be4637228c31/mfig002.jpg "The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library")
The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library
![The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0559668d-daba-4c9f-a8c1-9d3e588e69ed/mfig006.jpg "The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library")
The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library
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![The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/4e1b1036-8309-4263-9573-10b34ae0b55f/msch001.jpg "The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library")
The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library
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![The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/98bca7f9-e6ca-44a7-aeea-40d13370482a/msch002.jpg "The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library")
The Donor‐Stabilized Silylene Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis, Electronic Structure, and Reactivity - Junold - 2014 - Chemistry – A European Journal - Wiley Online Library
Small Molecule Activation by Two‐Coordinate Acyclic Silylenes - Fujimori - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library
