Specific Far Infrared Spectroscopic Properties of Phospholipids

Table 1

Summary of the tentative assignments presented in the text.

EPC (cm^−1)	PC (cm^−1)	PC D22 (cm^−1)	PC D35 (cm^−1)	PI (cm^−1)	EPG (cm^−1)	CL (cm^−1)	EPE (cm^−1)	PE (cm^−1)	ESM (cm^−1)	Tentative assignment
			542 (sh)							δ(CN^+(CD3)3)
575	575	575							577	δ(CN^+(CH3)3)
					559	560				𝛿oop(C–OH)
							552	555		δ(CN^+H3)
									548	𝛿oop(C–N–OH)
532	530	528 (sh)	527 (sh)		538	540	534	532		δ(O–P=O)
				521	517	521		511	519	δ(O–P–O)
505	505	503	507						507	δ(O–P–O)
									488
463	473	461	457	463	459	463	457	465	461	τ(C–C)n?
	426			416					411
382	368	376	392 (sh)				395	390		τ(CCN)
					355
				344						Inositol ring
				309			312	309	307
									267
		247	244							τ(C–CD3)
252	251			239	230	250	245	237	235	τ(C–CH3)
187	189	187	189		187	214	195	185	193	τ(C–CH2), τ(C–CD2),; hydrogen bonds
96	96	96	102	145				90	106	Hydrogen bonds