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$_{3x}$ ) > print |
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024 | 7 | _ | |a 10.1002/anie.202506406 |2 doi |
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041 | _ | _ | |a English |
082 | _ | _ | |a 540 |
100 | 1 | _ | |a Brüning, Lukas |0 P:(DE-H253)PIP1102685 |b 0 |e Corresponding author |
245 | _ | _ | |a High‐Pressure Synthesis of Crystalline Double‐Layer Carbon Nitride Networks Stabilized in Bi$_7$C$_{ 10}$N$_{18}$(N$_{3(1‐ x )}$O$_{3x}$ ) |
260 | _ | _ | |a Weinheim |c 2025 |b Wiley-VCH |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1756898330_1637420 |2 PUB:(DE-HGF) |
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500 | _ | _ | |a CommunicationFigure 4. Phonon dispersion for a) Bi 7 C 10 N20 O and b) Bi 7 C 10 N18 O 3 at a synthesis pressure of 34 GPa. All calculated vibrational frequencies are real,indicating lattice dynamical stability. Projected electronic density of states (PDOS) for c) Bi 7 C 10 N20 O and d) Bi 7 C 10 N18 O 3 at 34 GPa.AcknowledgementsM.B. acknowledges the support of Deutsche Forschungsge-meinschaft (DFG Emmy-Noether project BY112/2-1). |
520 | _ | _ | |a 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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773 | _ | _ | |a 10.1002/anie.202506406 |g Vol. 64, no. 35, p. e202506406 |0 PERI:(DE-600)2011836-3 |n 35 |p e202506406 |t Angewandte Chemie / International edition |v 64 |y 2025 |x 1433-7851 |
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