Home > Publications database > High‐Pressure Synthesis of Crystalline Double‐Layer Carbon Nitride Networks Stabilized in Bi$_7$C$_{ 10}$N$_{18}$(N$_{3(1‐ x )}$O$_{3x}$ ) |
Journal Article | PUBDB-2025-03815 |
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2025
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/anie.202506406 doi:10.3204/PUBDB-2025-03815
Abstract: Application of high-pressure conditions in chemical synthesis has proven to access a wide range of novel nitrogen-rich compounds and to overcome the stability of the dinitrogen molecule. In the present work, we report the high-pressurehigh-temperature (HPHT) synthesis of Bi$_7$C$_{ 10}$N$_{18}$(N$_{3(1‐ x )}$O$_{3x}$ ), which features double-layers of poly-N-(1,3,5-triazin-2-yl)-guanidine [C4 N6x- ]n and non-polymerized guanidinate anions CN 35- . The structure model was determined by means ofsynchrotron single-crystal X-ray diffraction and is fully corroborated by theoretical calculations. The poly-N-(1,3,5-triazin-2-yl)-guanidine illustrates an example of a 2D polymerized anionic C─N network and represents the first intermediatebetween highly charged CN 35− anions and fully condensed graphitic carbon nitride networks achieved by HPHT conditions.This opens a pathway to a widely varied family of hydrogen-free nitridocarbonates, which has the potential to develop intoan alternative synthesis route to classical polycondensation reactions
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