| dbo:abstract
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- The organic compound 3-pyridylnicotinamide (3-pna), also known as N-(pyridin-3-yl)nicotinamide, is a kinked dipodal dipyridine that is synthesized through the reaction of nicotinoyl chloride and 3-aminopyridine. The nitrogen atoms on its pyridine rings, like those of its isomer 4-pyridylnicotinamide, can donate their electron lone pairs to metal cations, allowing it to bridge metal centers and act as a bidentate ligand in coordination polymers. It can be used to synthesize polymers that have potentially useful gas adsorption properties. (en)
- 3-吡啶基烟酰胺（3-pna）是一种双足的双吡啶有机配体，可由烟酰氯和3-氨基吡啶的反应制备。其吡啶环上的氮原子，如其异构体上的，可以将其孤对电子配位至金属阳离子，允许其桥接金属中心并作为配位聚合物中的双齿配体。它可用于合成具有潜在应用可能的气体吸附性能的聚合物。 (zh)
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| dbo:alternativeName
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- 3-pna (en)
- N-(Pyridin-3-yl)nicotinamide (en)
- 3-pyridinecarboxamide, N-3-pyridinyl- (en)
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| dbo:iupacName
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- N-(Pyridin-3-yl)pyridine-3-carboxamide (en)
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- 5251 (xsd:nonNegativeInteger)
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| dbp:othernames
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- 3 (xsd:integer)
- N-nicotinamide (en)
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| dbp:pin
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- N-pyridine-3-carboxamide (en)
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| rdfs:comment
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- The organic compound 3-pyridylnicotinamide (3-pna), also known as N-(pyridin-3-yl)nicotinamide, is a kinked dipodal dipyridine that is synthesized through the reaction of nicotinoyl chloride and 3-aminopyridine. The nitrogen atoms on its pyridine rings, like those of its isomer 4-pyridylnicotinamide, can donate their electron lone pairs to metal cations, allowing it to bridge metal centers and act as a bidentate ligand in coordination polymers. It can be used to synthesize polymers that have potentially useful gas adsorption properties. (en)
- 3-吡啶基烟酰胺（3-pna）是一种双足的双吡啶有机配体，可由烟酰氯和3-氨基吡啶的反应制备。其吡啶环上的氮原子，如其异构体上的，可以将其孤对电子配位至金属阳离子，允许其桥接金属中心并作为配位聚合物中的双齿配体。它可用于合成具有潜在应用可能的气体吸附性能的聚合物。 (zh)
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| rdfs:label
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- 3-Pyridylnicotinamide (en)
- 3-吡啶基烟酰胺 (zh)
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- 3-Pyridylnicotinamide (en)
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