|
|
|
|
| LEADER |
01000caa a22002652c 4500 |
| 001 |
NLM343403218 |
| 003 |
DE-627 |
| 005 |
20250303135814.0 |
| 007 |
cr uuu---uuuuu |
| 008 |
231226s2022 xx |||||o 00| ||eng c |
| 024 |
7 |
|
|a 10.1021/acs.langmuir.2c01068
|2 doi
|
| 028 |
5 |
2 |
|a pubmed25n1144.xml
|
| 035 |
|
|
|a (DE-627)NLM343403218
|
| 035 |
|
|
|a (NLM)35819938
|
| 040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
| 041 |
|
|
|a eng
|
| 100 |
1 |
|
|a Zhang, Junjie
|e verfasserin
|4 aut
|
| 245 |
1 |
0 |
|a Molecular Design, Supramolecular Assembly, and Excellent Dye Adsorption Capacity of Natural Rigid Dehydroabietic Acid-Tailored Amide Organogelators
|
| 264 |
|
1 |
|c 2022
|
| 336 |
|
|
|a Text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
| 338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
| 500 |
|
|
|a Date Completed 27.07.2022
|
| 500 |
|
|
|a Date Revised 29.08.2022
|
| 500 |
|
|
|a published: Print-Electronic
|
| 500 |
|
|
|a Citation Status MEDLINE
|
| 520 |
|
|
|a It is very appealing to synthesize functional soft materials from natural and abundant plant diterpenes because they have conformationally rigid and chiral properties. Herein, dehydroabietic-based monoamide (DA-1) and diamide (DA-2) were designed by introducing device interactions, π-π stacking and hydrogen bonding, with an aromatic group, C═O, and N-H. DA-1 and DA-2 can be gelled in a mixed solvent and a single solvent, respectively. Several novel supramolecular organic gels including highly entangled three-dimensional networks composed of rods or fibers were constructed. Interestingly, DA-2 forms a helical structure that is right-handed under the cooperative control of the solvent and the rigid structure of rosin. Gel formation was primarily driven by hydrogen bonding, π-π stacking, and van der Waals force. Combined with Gaussian calculation and X-ray diffraction (XRD), we established pack patterns for each system, revealing the roles played by rosin and amide groups. Moreover, the carbon tetrachloride gel of DA-2 can effectively remove Congo red in an aqueous solution, and the removal rate can reach 98.4%. This research explores an efficient organic gel for adsorbing Congo red dye with the secretions of pine trees
|
| 650 |
|
4 |
|a Journal Article
|
| 650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
| 650 |
|
7 |
|a Abietanes
|2 NLM
|
| 650 |
|
7 |
|a Amides
|2 NLM
|
| 650 |
|
7 |
|a Gels
|2 NLM
|
| 650 |
|
7 |
|a Solvents
|2 NLM
|
| 650 |
|
7 |
|a dehydroabietic acid
|2 NLM
|
| 650 |
|
7 |
|a 0S5XP6S3AU
|2 NLM
|
| 650 |
|
7 |
|a Congo Red
|2 NLM
|
| 650 |
|
7 |
|a 3U05FHG59S
|2 NLM
|
| 700 |
1 |
|
|a Zhang, Ming
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Dong, Yuxuan
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Gu, Wanting
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Liu, Tong
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Xing, Xinwei
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Song, Jie
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Wang, Maogong
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Han, Chunrui
|e verfasserin
|4 aut
|
| 773 |
0 |
8 |
|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1985
|g 38(2022), 29 vom: 26. Juli, Seite 8918-8927
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnas
|
| 773 |
1 |
8 |
|g volume:38
|g year:2022
|g number:29
|g day:26
|g month:07
|g pages:8918-8927
|
| 856 |
4 |
0 |
|u http://dx.doi.org/10.1021/acs.langmuir.2c01068
|3 Volltext
|
| 912 |
|
|
|a GBV_USEFLAG_A
|
| 912 |
|
|
|a SYSFLAG_A
|
| 912 |
|
|
|a GBV_NLM
|
| 912 |
|
|
|a GBV_ILN_22
|
| 912 |
|
|
|a GBV_ILN_350
|
| 912 |
|
|
|a GBV_ILN_721
|
| 951 |
|
|
|a AR
|
| 952 |
|
|
|d 38
|j 2022
|e 29
|b 26
|c 07
|h 8918-8927
|