Ni() immobilized on poly(guanidine-triazine-sulfonamide) (PGTSA/Ni): a mesoporous nanocatalyst for synthesis of imines

Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which...

Full description

Saved in:
Bibliographic Details
Published inRSC advances Vol. 12; no. 53; pp. 34425 - 34437
Main Authors Ghiai, Ramin, Alavinia, Sedigheh, Ghorbani-Vaghei, Ramin, Gharakhani, Alireza
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 29.11.2022
The Royal Society of Chemistry
Subjects
Online AccessGet full text
ISSN2046-2069
2046-2069
DOI10.1039/d2ra06196a

Cover

Abstract Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe 3 O 4 magnetic nanoparticles (Fe 3 O 4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe 3 O 4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss. Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields.
AbstractList Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe 3 O 4 magnetic nanoparticles (Fe 3 O 4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe 3 O 4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss. Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields.
Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe3O4 magnetic nanoparticles (Fe3O4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe3O4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss.Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe3O4 magnetic nanoparticles (Fe3O4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe3O4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss.
Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe O magnetic nanoparticles (Fe O MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe O MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss.
Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe 3 O 4 magnetic nanoparticles (Fe 3 O 4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe 3 O 4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss.
Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various fields. This study reports a novel approach for synthesizing a novel porous polymer stabilizer through condensation polymerization in which Fe3O4 magnetic nanoparticles (Fe3O4 MNPs) are used as hard templates. Using this method allowed the facile and fast removal of the template and mesopores formation following the Fe3O4 MNPs. Different techniques were performed to characterize the structure of the polymer. Based on the obtained results, the obtained mesoporous polymeric network was multi-layered and consisted of repeating units of sulfonamide, triazine, and guanidine as a novel heterogeneous multifunctional support. Afterward, the new nickel organometallic complex was supported on its inner surface using the porous poly sulfonamide triazine guanidine (PGTSA/Ni). In this process, the obtained PGTSA/Ni nanocomposite was used as a heterogeneous catalyst in the synthesis of imines from amines. Since this reaction has an acceptorless dehydrogenation pathway, the hydrogen gas is released as its by-product. The synthesized nanocatalyst was structurally confirmed using different characterization modalities, including FT-IR, SEM, XRD, EDX, TEM, elemental mapping, ICP-AES, BET, and TGA. In addition, all products were obtained in high turnover frequency (TOF) and turnover number (TON). The corresponding results revealed the high selectivity and activity of the prepared catalyst through these coupling reactions. Overall, the synthesized nanocatalyst is useable for eight cycles with no considerable catalytic efficiency loss.
Author Alavinia, Sedigheh
Ghiai, Ramin
Ghorbani-Vaghei, Ramin
Gharakhani, Alireza
AuthorAffiliation Department of Organic Chemistry
Faculty of Chemistry
Bu-Ali Sina University
AuthorAffiliation_xml – name: Faculty of Chemistry
– name: Department of Organic Chemistry
– name: Bu-Ali Sina University
Author_xml – sequence: 1
  givenname: Ramin
  surname: Ghiai
  fullname: Ghiai, Ramin
– sequence: 2
  givenname: Sedigheh
  surname: Alavinia
  fullname: Alavinia, Sedigheh
– sequence: 3
  givenname: Ramin
  surname: Ghorbani-Vaghei
  fullname: Ghorbani-Vaghei, Ramin
– sequence: 4
  givenname: Alireza
  surname: Gharakhani
  fullname: Gharakhani, Alireza
BackLink https://www.ncbi.nlm.nih.gov/pubmed/36545623$$D View this record in MEDLINE/PubMed
BookMark eNptkt1rFDEUxYO02Nr2xXcl4MuuMDbfmfggLFWrUFrR-hwyM0mbMpNsk5nC9q836_bLYl5yIb977rmcvAJbIQYLwGuMPmBE1WFHkkECK2FegF2CmKgIEmrrSb0DDnK-QuUIjonAL8EOFZxxQeguuDn1szn0wxAb3_tb28EY4DL2q9nFZILvfLDVmLy5XRd56l0MZvCdncPZj-PzX4vDUz__CA0cbI7LmOKUYTAhtmY0_SqP0MUE8yqMlzb7DKMro4pS3gfbzvTZHtzde-D31y_nR9-qk7Pj70eLk6plpB6rjqmuIcQ1jTBGUUFJ3XbMSqkQc7VrGHKMOswoNphxy4klRDSYdzVVTChJ98Cnje5yagbbtTaMyfR6mfxg0kpH4_W_L8Ff6ot4o5VEStaiCMzuBFK8nmwe9eBza_veBFuW1URyiQXBkhf03TP0Kk4plPUKxWSNJOeqUG-fOnqwch9JAdAGaFPMOVmnWz-a0ce1Qd9rjPQ6eP2Z_Fz8DX5RWt4_a7lX_S_8ZgOn3D5wj7-I_gG0FreJ
CitedBy_id crossref_primary_10_1039_D3TA06022E
crossref_primary_10_1016_j_jpcs_2024_112386
crossref_primary_10_1016_j_molstruc_2023_136635
crossref_primary_10_1016_j_carpta_2025_100665
crossref_primary_10_1016_j_molstruc_2023_136227
crossref_primary_10_1002_aoc_7831
crossref_primary_10_1039_D3NJ00416C
crossref_primary_10_1039_D3RA00049D
crossref_primary_10_1016_j_jorganchem_2023_122729
crossref_primary_10_1039_D3RA03058J
crossref_primary_10_1016_j_mtcomm_2024_109320
crossref_primary_10_1039_D4NA00151F
crossref_primary_10_1007_s10904_024_03519_0
Cites_doi 10.1021/jo00287a028
10.1002/aoc.5400
10.1002/jhet.3904
10.1016/j.matchemphys.2022.126915
10.1016/j.jpcs.2020.109573
10.1002/chem.201804402
10.1002/asia.201900843
10.1016/j.jiec.2021.02.001
10.1016/j.mtchem.2020.100308
10.1002/slct.202103856
10.1055/s-0037-1611851
10.1002/aoc.6823
10.1039/D1GC02505H
10.1016/j.ijbiomac.2022.04.140
10.1021/acs.orglett.6b02697
10.1016/j.jorganchem.2021.121971
10.1039/C7OB02670F
10.1016/j.apsusc.2019.02.250
10.1016/j.tetlet.2013.07.007
10.1002/ejoc.201901462
10.1016/j.jenvman.2021.112360
10.1002/ejoc.202100946
10.1021/jacs.7b07167
10.1021/acssuschemeng.9b00619
10.1038/nprot.2015.025
10.1007/s10562-016-1789-3
10.1007/s10934-021-01104-1
10.1038/s41598-022-05411-8
10.1016/j.poly.2018.10.054
10.1021/jo501601u
10.1039/C9GC03655E
10.1002/aoc.6905
10.1021/acs.orglett.9b01016
10.1016/j.molstruc.2022.133860
10.1007/s10934-017-0508-9
10.1002/ange.201801289
10.1039/C9CY00009G
10.1002/aoc.6656
10.1007/s11164-019-03930-0
10.1038/s41598-021-94846-6
10.1002/aoc.5449
10.1002/aoc.4127
10.1016/j.fuel.2016.07.004
10.1002/cctc.201800677
10.1038/s41467-018-02930-9
10.1021/jacs.0c07784
10.1139/cjc-2021-0250
10.1002/aoc.5379
10.1002/chem.201900737
10.1039/C8SC03969K
10.1039/D0NJ02215B
10.1039/C8RA10212K
10.1039/D1GC02062E
10.1039/C7CY00432J
ContentType Journal Article
Copyright This journal is © The Royal Society of Chemistry.
Copyright Royal Society of Chemistry 2022
This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry
Copyright_xml – notice: This journal is © The Royal Society of Chemistry.
– notice: Copyright Royal Society of Chemistry 2022
– notice: This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry
DBID AAYXX
CITATION
NPM
7SR
8BQ
8FD
JG9
7X8
5PM
DOI 10.1039/d2ra06196a
DatabaseName CrossRef
PubMed
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
METADEX
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
PubMed

CrossRef
Materials Research Database
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2046-2069
EndPage 34437
ExternalDocumentID PMC9709786
36545623
10_1039_D2RA06196A
d2ra06196a
Genre Journal Article
GroupedDBID -JG
0-7
0R~
AAGNR
AAIWI
ABGFH
ACGFS
ADBBV
ADMRA
AENEX
AFVBQ
AGRSR
AGSTE
ALMA_UNASSIGNED_HOLDINGS
ANUXI
ASKNT
AUDPV
BCNDV
BLAPV
BSQNT
C6K
EBS
EE0
EF-
GROUPED_DOAJ
H13
HZ~
H~N
J3I
O9-
OK1
R7C
R7G
RCNCU
RPM
RPMJG
RRC
RSCEA
RVUXY
SLH
SMJ
ZCN
53G
AAFWJ
AAHBH
AAJAE
AARTK
AAWGC
AAXHV
AAYXX
ABEMK
ABIQK
ABPDG
ABXOH
AEFDR
AESAV
AFLYV
AFPKN
AGEGJ
AHGCF
AKBGW
APEMP
CITATION
M~E
PGMZT
NPM
7SR
8BQ
8FD
JG9
7X8
5PM
ID FETCH-LOGICAL-c428t-d49db22fbb6aa936328cd4e77904f8fb40f43f1431a145e52e226b15d83946973
ISSN 2046-2069
IngestDate Thu Aug 21 18:39:08 EDT 2025
Thu Sep 04 16:05:52 EDT 2025
Mon Jun 30 06:59:58 EDT 2025
Thu Jan 02 22:36:27 EST 2025
Tue Jul 01 04:20:24 EDT 2025
Thu Apr 24 23:05:16 EDT 2025
Fri Dec 09 04:10:57 EST 2022
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 53
Language English
License This journal is © The Royal Society of Chemistry.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c428t-d49db22fbb6aa936328cd4e77904f8fb40f43f1431a145e52e226b15d83946973
Notes https://doi.org/10.1039/d2ra06196a
Electronic supplementary information (ESI) available. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-8322-6299
OpenAccessLink http://dx.doi.org/10.1039/d2ra06196a
PMID 36545623
PQID 2747807559
PQPubID 2047525
PageCount 13
ParticipantIDs proquest_miscellaneous_2757162175
pubmed_primary_36545623
crossref_primary_10_1039_D2RA06196A
proquest_journals_2747807559
rsc_primary_d2ra06196a
crossref_citationtrail_10_1039_D2RA06196A
pubmedcentral_primary_oai_pubmedcentral_nih_gov_9709786
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-11-29
PublicationDateYYYYMMDD 2022-11-29
PublicationDate_xml – month: 11
  year: 2022
  text: 2022-11-29
  day: 29
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: Cambridge
PublicationTitle RSC advances
PublicationTitleAlternate RSC Adv
PublicationYear 2022
Publisher Royal Society of Chemistry
The Royal Society of Chemistry
Publisher_xml – name: Royal Society of Chemistry
– name: The Royal Society of Chemistry
References Martin-Montero (D2RA06196A/cit10/1) 2019; 21
Beaucamp (D2RA06196A/cit29/1) 2021; 23
Alavinia (D2RA06196A/cit35/1) 2022; 293
Jagadeesh (D2RA06196A/cit14/1) 2015; 10
Parua (D2RA06196A/cit12/1) 2018; 16
Wang (D2RA06196A/cit9/1) 2017; 139
Mohammadi (D2RA06196A/cit17/1) 2021; 97
Bottaro (D2RA06196A/cit55/1) 2019
Wu (D2RA06196A/cit16/1) 2021; 23
Alavinia (D2RA06196A/cit34/1) 2020; 146
Rahimi (D2RA06196A/cit40/1) 2022; 7
Atilgan (D2RA06196A/cit33/1) 2020; 142
Harry (D2RA06196A/cit8/1) 2019; 9
Babamoradi (D2RA06196A/cit38/1) 2022; 209
Liu (D2RA06196A/cit13/1) 2019; 7
Patterson (D2RA06196A/cit53/1) 2021; 2021
Rahimi (D2RA06196A/cit6/1) 2021; 28
Li (D2RA06196A/cit26/1) 2020; 17
Sonai Muthu (D2RA06196A/cit30/1) 2019; 480
Ramish (D2RA06196A/cit22/1) 2022; 12
Gopalaiah (D2RA06196A/cit46/1) 2016; 146
Yuan (D2RA06196A/cit28/1) 2018; 130
Rai (D2RA06196A/cit48/1) 2006; 83
Azizi (D2RA06196A/cit3/1) 2018; 10
Dai (D2RA06196A/cit11/1) 2017; 7
Hussain-Khil (D2RA06196A/cit23/1) 2021; 11
Jiang (D2RA06196A/cit47/1) 2014; 79
Li (D2RA06196A/cit15/1) 2020; 22
Wu (D2RA06196A/cit37/1) 2016; 184
Azizi (D2RA06196A/cit1/1) 2019; 25
Koolivand (D2RA06196A/cit21/1) 2022; 36
Monda (D2RA06196A/cit4/1) 2018; 24
Ghorbani-Vaghei (D2RA06196A/cit44/1) 2018; 32
Ghorbani-Choghamarani (D2RA06196A/cit43/1) 2019; 45
Silverberg (D2RA06196A/cit51/1) 2020; 57
Ghobakhloo (D2RA06196A/cit20/1) 2022; 36
Sobhani (D2RA06196A/cit50/1) 2019; 9
Samuelsen (D2RA06196A/cit2/1) 2019; 10
Geherty (D2RA06196A/cit52/1) 2013; 54
Kazemi (D2RA06196A/cit18/1) 2020; 34
Goriya (D2RA06196A/cit5/1) 2016; 18
Alavinia (D2RA06196A/cit36/1) 2020; 44
Takallou (D2RA06196A/cit54/1) 2020; 34
Galván (D2RA06196A/cit45/1) 2019; 51
Shekarlab (D2RA06196A/cit7/1) 2021; 949
Ghorbani-Choghamarani (D2RA06196A/cit42/1) 2019; 158
Singh (D2RA06196A/cit25/1) 2018; 25
Strekowski (D2RA06196A/cit49/1) 1989; 54
Alavinia (D2RA06196A/cit39/1) 2022; 1270
Babamoradi (D2RA06196A/cit41/1) 2022; 100
Alavinia (D2RA06196A/cit24/1) 2020; 34
Fang (D2RA06196A/cit27/1) 2018; 9
Waheed (D2RA06196A/cit31/1) 2021; 287
Mohammadi (D2RA06196A/cit19/1) 2022
Ma (D2RA06196A/cit32/1) 2019; 14
References_xml – volume: 54
  start-page: 6120
  year: 1989
  ident: D2RA06196A/cit49/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00287a028
– volume: 34
  start-page: e5400
  year: 2020
  ident: D2RA06196A/cit18/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.5400
– volume: 57
  start-page: 1797
  year: 2020
  ident: D2RA06196A/cit51/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.3904
– volume: 293
  start-page: 126915
  year: 2022
  ident: D2RA06196A/cit35/1
  publication-title: Mater. Chem. Phys.
  doi: 10.1016/j.matchemphys.2022.126915
– volume: 146
  start-page: 109573
  year: 2020
  ident: D2RA06196A/cit34/1
  publication-title: J. Phys. Chem. Solids
  doi: 10.1016/j.jpcs.2020.109573
– volume: 24
  start-page: 17832
  year: 2018
  ident: D2RA06196A/cit4/1
  publication-title: Chem.–Eur. J.
  doi: 10.1002/chem.201804402
– volume: 14
  start-page: 3502
  year: 2019
  ident: D2RA06196A/cit32/1
  publication-title: Chem.–Asian J.
  doi: 10.1002/asia.201900843
– volume: 97
  start-page: 1
  year: 2021
  ident: D2RA06196A/cit17/1
  publication-title: J. Ind. Eng. Chem.
  doi: 10.1016/j.jiec.2021.02.001
– volume: 17
  start-page: 100308
  year: 2020
  ident: D2RA06196A/cit26/1
  publication-title: Mater. Today Chem.
  doi: 10.1016/j.mtchem.2020.100308
– volume: 7
  start-page: e202103856
  year: 2022
  ident: D2RA06196A/cit40/1
  publication-title: ChemistrySelect
  doi: 10.1002/slct.202103856
– volume: 51
  start-page: 3625
  year: 2019
  ident: D2RA06196A/cit45/1
  publication-title: Synthesis
  doi: 10.1055/s-0037-1611851
– volume: 36
  start-page: e6823
  year: 2022
  ident: D2RA06196A/cit20/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.6823
– volume: 23
  start-page: 6675
  year: 2021
  ident: D2RA06196A/cit16/1
  publication-title: Green Chem.
  doi: 10.1039/D1GC02505H
– volume: 209
  start-page: 1542
  year: 2022
  ident: D2RA06196A/cit38/1
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2022.04.140
– volume: 18
  start-page: 5174
  year: 2016
  ident: D2RA06196A/cit5/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b02697
– volume: 949
  start-page: 121971
  year: 2021
  ident: D2RA06196A/cit7/1
  publication-title: J. Organomet. Chem.
  doi: 10.1016/j.jorganchem.2021.121971
– volume: 16
  start-page: 274
  year: 2018
  ident: D2RA06196A/cit12/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C7OB02670F
– volume: 480
  start-page: 186
  year: 2019
  ident: D2RA06196A/cit30/1
  publication-title: Appl. Surf. Sci.
  doi: 10.1016/j.apsusc.2019.02.250
– volume: 54
  start-page: 4934
  year: 2013
  ident: D2RA06196A/cit52/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2013.07.007
– start-page: 7164
  year: 2019
  ident: D2RA06196A/cit55/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201901462
– volume: 287
  start-page: 112360
  year: 2021
  ident: D2RA06196A/cit31/1
  publication-title: J. Environ. Manage.
  doi: 10.1016/j.jenvman.2021.112360
– volume: 2021
  start-page: 6737
  year: 2021
  ident: D2RA06196A/cit53/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.202100946
– volume: 139
  start-page: 13499
  year: 2017
  ident: D2RA06196A/cit9/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b07167
– volume: 7
  start-page: 11267
  year: 2019
  ident: D2RA06196A/cit13/1
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.9b00619
– volume: 10
  start-page: 548
  year: 2015
  ident: D2RA06196A/cit14/1
  publication-title: Nat. Protoc.
  doi: 10.1038/nprot.2015.025
– volume: 146
  start-page: 1648
  year: 2016
  ident: D2RA06196A/cit46/1
  publication-title: Catal. Lett.
  doi: 10.1007/s10562-016-1789-3
– volume: 28
  start-page: 1643
  year: 2021
  ident: D2RA06196A/cit6/1
  publication-title: J. Porous Mater.
  doi: 10.1007/s10934-021-01104-1
– volume: 12
  start-page: 1479
  year: 2022
  ident: D2RA06196A/cit22/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-022-05411-8
– volume: 83
  start-page: 208
  year: 2006
  ident: D2RA06196A/cit48/1
  publication-title: J. Indian Chem. Soc.
– volume: 158
  start-page: 25
  year: 2019
  ident: D2RA06196A/cit42/1
  publication-title: Polyhedron
  doi: 10.1016/j.poly.2018.10.054
– volume: 79
  start-page: 8768
  year: 2014
  ident: D2RA06196A/cit47/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo501601u
– volume: 22
  start-page: 582
  year: 2020
  ident: D2RA06196A/cit15/1
  publication-title: Green Chem.
  doi: 10.1039/C9GC03655E
– start-page: e6905
  year: 2022
  ident: D2RA06196A/cit19/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.6905
– volume: 21
  start-page: 2947
  year: 2019
  ident: D2RA06196A/cit10/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b01016
– volume: 1270
  start-page: 133860
  year: 2022
  ident: D2RA06196A/cit39/1
  publication-title: J. Mol. Struct.
  doi: 10.1016/j.molstruc.2022.133860
– volume: 25
  start-page: 965
  year: 2018
  ident: D2RA06196A/cit25/1
  publication-title: J. Porous Mater.
  doi: 10.1007/s10934-017-0508-9
– volume: 130
  start-page: 5810
  year: 2018
  ident: D2RA06196A/cit28/1
  publication-title: Angew. Chem.
  doi: 10.1002/ange.201801289
– volume: 9
  start-page: 1726
  year: 2019
  ident: D2RA06196A/cit8/1
  publication-title: Catal. Sci. Technol.
  doi: 10.1039/C9CY00009G
– volume: 36
  start-page: e6656
  year: 2022
  ident: D2RA06196A/cit21/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.6656
– volume: 45
  start-page: 5705
  year: 2019
  ident: D2RA06196A/cit43/1
  publication-title: Res. Chem. Intermed.
  doi: 10.1007/s11164-019-03930-0
– volume: 11
  start-page: 15657
  year: 2021
  ident: D2RA06196A/cit23/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-021-94846-6
– volume: 34
  start-page: e5449
  year: 2020
  ident: D2RA06196A/cit24/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.5449
– volume: 32
  start-page: e4127
  year: 2018
  ident: D2RA06196A/cit44/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.4127
– volume: 184
  start-page: 128
  year: 2016
  ident: D2RA06196A/cit37/1
  publication-title: Fuel
  doi: 10.1016/j.fuel.2016.07.004
– volume: 10
  start-page: 3703
  year: 2018
  ident: D2RA06196A/cit3/1
  publication-title: ChemCatChem
  doi: 10.1002/cctc.201800677
– volume: 9
  start-page: 521
  year: 2018
  ident: D2RA06196A/cit27/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-018-02930-9
– volume: 142
  start-page: 18554
  year: 2020
  ident: D2RA06196A/cit33/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c07784
– volume: 100
  start-page: 412
  year: 2022
  ident: D2RA06196A/cit41/1
  publication-title: Can. J. Chem.
  doi: 10.1139/cjc-2021-0250
– volume: 34
  start-page: e5379
  year: 2020
  ident: D2RA06196A/cit54/1
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.5379
– volume: 25
  start-page: 6439
  year: 2019
  ident: D2RA06196A/cit1/1
  publication-title: Chem.–Eur. J.
  doi: 10.1002/chem.201900737
– volume: 10
  start-page: 1150
  year: 2019
  ident: D2RA06196A/cit2/1
  publication-title: Chem. Sci.
  doi: 10.1039/C8SC03969K
– volume: 44
  start-page: 13062
  year: 2020
  ident: D2RA06196A/cit36/1
  publication-title: New J. Chem.
  doi: 10.1039/D0NJ02215B
– volume: 9
  start-page: 1362
  year: 2019
  ident: D2RA06196A/cit50/1
  publication-title: RSC Adv.
  doi: 10.1039/C8RA10212K
– volume: 23
  start-page: 5696
  year: 2021
  ident: D2RA06196A/cit29/1
  publication-title: Green Chem.
  doi: 10.1039/D1GC02062E
– volume: 7
  start-page: 2506
  year: 2017
  ident: D2RA06196A/cit11/1
  publication-title: Catal. Sci. Technol.
  doi: 10.1039/C7CY00432J
SSID ssj0000651261
Score 2.440969
Snippet Mesoporous materials have been the subject of intense research regarding their unique structural and textural properties and successful applications in various...
SourceID pubmedcentral
proquest
pubmed
crossref
rsc
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 34425
SubjectTerms Amines
Atomic emission spectroscopy
Catalysts
Chemical reactions
Chemical synthesis
Chemistry
Condensates
Condensation polymerization
Dehydrogenation
Emission analysis
Imines
Inductively coupled plasma
Iron oxides
Multilayers
Nanocomposites
Nanoparticles
Polymers
Selectivity
Stabilizers (agents)
Sulfonamides
Title Ni() immobilized on poly(guanidine-triazine-sulfonamide) (PGTSA/Ni): a mesoporous nanocatalyst for synthesis of imines
URI https://www.ncbi.nlm.nih.gov/pubmed/36545623
https://www.proquest.com/docview/2747807559
https://www.proquest.com/docview/2757162175
https://pubmed.ncbi.nlm.nih.gov/PMC9709786
Volume 12
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dbtMwFLa6cQE3iL9BYCAjuGiFwprYcRLuorF1QqOgtUW7i5zGWSNKMvUHaRUXvAMPw_vwJJwTJ2mqTgi4iVLHsdOcr_Z33OPvEPLSgXJ_7ChTyLE0eSK56UWWMIVC8u6ySDDcjfy-L05G_N25c95q_WxELS0X0evx6tp9Jf9jVSgDu-Iu2X-wbN0oFMA52BeOYGE4_pWN-3Cvl6bo2afQK8a5roBAgkEvc8wg7V0sZZbGqCVaxjQwzNKxahbMl9Mkx6z0qL_rI-H82BsOAngobN3Xm6G_qHkORL1Qc5VZXqz5XM0XRYzi_CoDElnqmmCOsDIqsVL9HhxWgQY1fe9NUp0F-wz6rdEZTOXXNNPBuwOYUy8marK-I59F8F3MTxKKt-_toe7054lOUPUqmMJAvpLNFQ1whi3LtNfjpl43qYJWi6CUMvWdnrOKwdEGvx6woNO81CO53UCswxrjMuNc768uJ3n4rLVmtmaQLkMB1tieSWA6vmjMk1VsQP9DeDw6PQ2HR-fDHXLDdoG0NXx5TQGARwmrksNl_sG6wU0CtOXVbAfn7syqXDQF5xneIbdLZ4UGGnl3SUtl98jN-kXdJ9_6aTtNO7SBPppnFNHXrrH36_uPCnVw2sBbh7YLrB30084bKukaZbSJMgooozXKaJ5QjbIHZHR8NDw8Mct8HuYYnNyFGXM_jmw7iSIhpc8EszFzlkLFS554ScS7CWcJEHhLWtxRjq3AN4gsJwYSz4Xvsj2ym-WZekQo-PUx9zh3mUq4EwmPR9YYmnJYzLtWrAzSqV5yOC7F7jHnyjQsgi6YH761z4LCIIFBXtR1L7XEy7W19itbheUQMA9xSQfVvB3fIM_ry2AD_NdNZgpeGNRxUKUNaLpBHmrT1t0wgQ6MzQzibhi9roDi75tXsnRSiMD7Lu7AEgbZA3jU9dcwe_zn531Cbq1_evtkdzFbqqdArxfRswLKvwFk7dWE
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Ni%28ii%29+immobilized+on+poly%28guanidine%E2%80%93triazine%E2%80%93sulfonamide%29+%28PGTSA%2FNi%29%3A+a+mesoporous+nanocatalyst+for+synthesis+of+imines&rft.jtitle=RSC+advances&rft.au=Ghiai%2C+Ramin&rft.au=Alavinia%2C+Sedigheh&rft.au=Ghorbani-Vaghei%2C+Ramin&rft.au=Gharakhani%2C+Alireza&rft.date=2022-11-29&rft.pub=Royal+Society+of+Chemistry&rft.eissn=2046-2069&rft.volume=12&rft.issue=53&rft.spage=34425&rft.epage=34437&rft_id=info:doi/10.1039%2Fd2ra06196a&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2046-2069&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2046-2069&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2046-2069&client=summon