Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Luka Fotović"'
Autor:
Krešimir Molčanov, Valentina Milašinović, Biserka Kojić-Prodić, Nadica Maltar-Strmečki, Jiangyang You, Ana Šantić, Lidija Kanižaj, Vladimir Stilinović, Luka Fotović
Publikováno v:
IUCrJ, Vol 9, Iss 4, Pp 449-467 (2022)
Multicentre two-electron (mc/2e or `pancake bonding') bonding between 7,7,8,8-tetracyanoquinodimethane (TCNQ) radical anions was studied on its 14 novel salts with planar organic cations. The formal charges of the TCNQδ− moieties are −1/2 and
Externí odkaz:
https://doaj.org/article/161d531fff9b4b9599272de6d5891658
Autor:
Luka Fotović, Vladimir Stilinović
Publikováno v:
Crystals, Vol 11, Iss 10, p 1240 (2021)
We performed a structural study of N-alkylated halogenopyridinium cations to examine whether choice of the N-substituent has any considerable effect on the halogen bonding capability of the cations. For that purpose, we prepared a series of N-ethyl-3
Externí odkaz:
https://doaj.org/article/f73acb7c383f4a31931a564d09f98742
Publikováno v:
Crystals, Vol 11, Iss 5, p 529 (2021)
In order to study the proclivity of primary amine groups to act as halogen bond acceptors, three aromatic diamines (p-phenylenediamine (pphda), benzidine (bnzd) and o-tolidine (otol)) were cocrystallised with three perfluorinated iodobenzenes (1,4-te
Externí odkaz:
https://doaj.org/article/305e51bfc4cf45808e0e55b11cf06f88
Publikováno v:
Crystal Growth & Design. 22:7508-7517
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::773b4ed4e1863df11fffab75375b854e
https://doi.org/10.1021/acs.cgd.2c01055
https://doi.org/10.1021/acs.cgd.2c01055
Publikováno v:
Crystal Growth & Design. 22:987-992
Seven cocrystals of pyridone and perfluorinated halocarbons have been prepared. In all cases pairs of pyridone molecules are connected into dimers by two N–H···O hydrogen bonds, forming the characteristic pyridone homosynthon of R22(8) topology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e08ffa3299e37311b783c8ef744a1f5
https://doi.org/10.1021/acs.cgd.1c01424
https://doi.org/10.1021/acs.cgd.1c01424
In order to study the potential of Keggin type polyoxometalate anions to act as halogen bond acceptors we have prepared a series of 10 halogen- bonded compounds starting from phosphomolybdic and phosphotungstic acid and halogenopyridinium cations as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b661bfb467e78af35a44e6916547ea83
https://www.bib.irb.hr/1270185
https://www.bib.irb.hr/1270185
Publikováno v:
CrystEngComm. 22:8142-8150
In order to examine the possibility of controlling formation of hydrogen bonded hexacyanoferrous networks through combination of hydrogen and halogen bonding, seven new crystalline compounds were obtained by reacting hexacyanoferrous acid (H4[Fe(CN)6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8412614808f873c69acf9b4ca522d8e8
https://doi.org/10.1039/d0ce01359e
https://doi.org/10.1039/d0ce01359e
Autor:
Vladimir Stilinović, Luka Fotović
Publikováno v:
CrystEngComm. 22:4039-4046
In order to study halogenide anions simultaneously acting as hydrogen bond and halogen bond acceptors, we have prepared and crystallised halogenide salts (chlorides, bromides and iodides) of the three isomers of iodopyridine, 2-iodopyridine (2-IPy),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c60f3f3e4bf66891118e25865637abe
https://doi.org/10.1039/d0ce00534g
https://doi.org/10.1039/d0ce00534g
Six N-(4-halogenobenzyl)-3-halogenopyridinium cations were prepared by reacting meta-halogenopyridines (Cl, Br, and I) with (4-halogenobenzyl) bromides (Br and I) and were isolated as bromide salts, which were further used to obtain iodides and chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a529e5e60d94196b904588ef5d35fed
https://doi.org/10.1021/acs.cgd.1c01285
https://doi.org/10.1021/acs.cgd.1c01285
Publikováno v:
Crystal growthdesign. 22(2)
Six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd0be757f9e0fd842886d03948cfcf74
https://pubmed.ncbi.nlm.nih.gov/35250388
https://pubmed.ncbi.nlm.nih.gov/35250388