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Hydrogen bonding and polymorphism of amino alcohol salts with quinaldinate : structural study
ID
Podjed, Nina
(
Avtor
),
ID
Modec, Barbara
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(3,53 MB)
MD5: 7AD03DB7EC591DB5C737B1EEEB9E0B4D
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1420-3049/27/3/996
Galerija slik
Izvleček
Three amino alcohols, 3-amino-1-propanol (abbreviated as 3a1pOH), 2-amino-1-butanol (2a1bOH), and 2-amino-2-methyl-1-propanol (2a2m1pOH), were reacted with quinoline-2-carboxylic acid, known as quinaldinic acid. This combination yielded three salts, (3a1pOHH)quin (1, 3a1pOHH$^+$ = protonated 3-amino-1-propanol, quin$^−$ = anion of quinaldinic acid), (2a1bOHH)quin (2, 2a1bOHH$^+$ = protonated 2-amino-1-butanol), and (2a2m1pOHH)quin (3, 2a2m1pOHH$^+$ = protonated 2-amino-2-methyl-1-propanol). The 2-amino-1-butanol and 2-amino-2-methyl-1-propanol systems produced two polymorphs each, labeled 2a/2b and 3a/3b, respectively. The compounds were characterized by X-ray structure analysis on single-crystal. The crystal structures of all consisted of protonated amino alcohols with NH$_3$$^+$ moiety and quinaldinate anions with carboxylate moiety. The used amino alcohols contained one OH and one NH$_2$ functional group, both prone to participate in hydrogen bonding. Therefore, similar connectivity patterns were expected. This proved to be true to some extent as all structures contained the NH$_3$$^+$···$^−$OOC heterosynthon. Nevertheless, different hydrogen bonding and π···π stacking interactions were observed, leading to distinct connectivity motifs. The largest difference in hydrogen bonding occurred between polymorphs 3a and 3b, as they had only one heterosynton in common.
Jezik:
Angleški jezik
Ključne besede:
hydrogen bond
,
synthon
,
crystal structure
,
polymorphism
,
amino alcohols
,
quinaldinic acid
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2022
Št. strani:
12 str.
Številčenje:
Vol. 27, iss. 3, art. 996
PID:
20.500.12556/RUL-137360
UDK:
544.142.4
ISSN pri članku:
1420-3049
DOI:
10.3390/molecules27030996
COBISS.SI-ID:
96752899
Datum objave v RUL:
14.06.2022
Število ogledov:
816
Število prenosov:
106
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Molecules
Skrajšan naslov:
Molecules
Založnik:
MDPI
ISSN:
1420-3049
COBISS.SI-ID:
18462981
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
01.02.2022
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
vodikova vez
,
sinton
,
kristalna struktura
,
polimorfizem
,
amino alkoholi
,
kinaldinska kislina
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Program financ.:
Young researchers
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0134
Naslov:
Kemija za trajnostni razvoj
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