0000000001299266
AUTHOR
Mario Cetina
Synthesis of [5]Rotaxanes Containing Bi- and Tridentate Coordination Sites in the Axis
A new example of a linear [5]rotaxane has been synthesized by using the traditional "gathering-and-threading" approach but based on an unusual axle incorporating a symmetrical bis(bidentate) chelating fragment built on a 4,7-phenanthroline core. The stoppering reaction is particularly noteworthy since, instead of using a trivial bulky stopper as precursor to the blocking group, two semistoppered copper-complexed [2]pseudorotaxanes (namely [2]semirotaxanes) are used, which leads to the desired [5]rotaxane in good yield. The efficiency of the method relies on the use of "click" chemistry, with its very mild conditions, and on the protection by a transition-metal (copper(I)) of the various coo…
Recognition of N-Alkyl- and N-Aryl-Acetamides by N-Alkyl Ammonium Resorcinarene Chlorides
N-alkyl ammonium resorcinarene chlorides are stabilized by an intricate array of intra- and intermolecular hydrogen bonds that leads to cavitand-like structures. Depending on the upper-rim substituents, self-inclusion was observed in solution and in the solid state. The self-inclusion can be disrupted at higher temperatures, whereas in the presence of small guests the self-included dimers spontaneously reorganize to 1:1 host-guest complexes. These host compounds show an interesting ability to bind a series of N-alkyl acetamide guests through intermolecular hydrogen bonds involving the carbonyl oxygen (C=O) atoms and the amide (NH) groups of the guests, the chloride anions (Cl(-)) and ammoni…
Amidino substituted 2-aminophenols: biologically important building blocks for the amidino-functionalization of 2-substituted benzoxazoles
Unlike the closely related and widely investigated amidino-substituted benzimidazoles and benzothiazoles with a range of demonstrated biological activities, the matching benzoxazole analogues still remain a largely understudied and not systematically evaluated class of compounds. To address this challenge, we utilized the Pinner reaction to convert isomeric cyano-substituted 2- aminophenols into their amidine derivatives, which were isolated as hydrochlorides and/or zwitterions, and whose structure was confirmed by single crystal X-ray diffraction. The key step during the Pinner synthesis of the crucial carboximidate intermediates was characterized through mechanistic DFT calculations, with…
Neutral Organometallic Halogen Bond Acceptors: Halogen Bonding in Complexes of PCPPdX (X = Cl, Br, I) with Iodine (I(2)), 1,4-Diiodotetrafluorobenzene (F4DIBz), and 1,4-Diiodooctafluorobutane (F8DIBu).
The behavior of a sterically crowded neutral pincer {2,6-bis[(di-t-butylphosphino)methyl]-phenyl}palladium (PCPPd) halides, PCPPdX (X = Cl, Br or I), as XB acceptors with strong halogen bond (XB) donors, iodine (I2), 1,4-diiodotetrafluorobenzene (F4DIBz), and 1,4-diiodooctafluorobutane (F8DIBu) were studied in the solid state. The co-crystallization experiments afforded high-quality single crystals of XB complexes PCPPdCl–I2 (1a), PCPPdBr–I2 (2a), PCPPdI–I2(3a), PCPPdCl–F4DIBz (1b), PCPPdBr–F4DIBz (2b), and PCPPdBr–F8DIBu (2c). The 1:1 iodine complexes (1a, 2a, and 3a) all showed a strong halogen bonding interaction, the reduction of the sum of the van der Waals radii of halogen to iodine b…
Luminescent alkynyl-gold(i) coumarin derivatives and their biological activity
The synthesis and characterization of three propynyloxycoumarins are reported in this work together with the formation of three different series of gold(i) organometallic complexes. Neutral complexes are constituted by water soluble phosphines (PTA and DAPTA) which confer water solubility to them. The X-ray crystal structure of 7-(prop-2-in-1-yloxy)-1-benzopyran-2-one and its corresponding dialkynyl complex is also shown and the formation of rectangular dimers for the gold derivative in the solid state can be observed. A detailed analysis of the absorption and emission spectra of both ligands and complexes allows us to attribute the luminescent behaviour to the coumarin organic ligand. More…
Halogen Bonded Analogues of Deep Cavity Cavitands
The first examples of halogen bonded analogues of deep cavity cavitands with guest binding properties, formed between N-alkyl ammonium resorcinarene halides as acceptors and bromotrichloromethane as the donor, are reported in the solid state and in solution.
From self-inclusion and host-guest complexes to channel structures
Various supramolecular interactions are applied as driving forces in self-assembly and molecular recognition processes. Single crystal X-ray diffraction method is especially important for solid-state studies of non-covalent interactions as it reveals their influence on the molecular and supramolecular structures. This paper discusses structures of two completely different types of compounds in which a variety of intermolecular interactions are involved. It will be shown that strong and weak intermolecular hydrogen bonds in N-alkylammonium resorcinarene salts, depending on the type of anion, inclusion of resorcinarene upper rim pendant group or solvent molecules into the cavity, strongly aff…
Hydrogen bond-stabilised N-alkylammonium resorcinarene halide cavitands
A family of hydrogen bond-stabilised N-alkylammonium resorcinarene chloride and bromide cavitands were synthesised and characterised with 1H NMR and ESI mass spectrometry. The seven compounds exhibit interestingly either self-inclusion or guest complexation in the solid state evidenced by single crystal X-ray diffraction. The four dimers show self-inclusion of the upper rim propyl chains and consist of two hydrogen-bonded resorcinarene tetracations and six halide anions, while the remaining two halide anions are located in between the dimers linking them via hydrogen bonding. Small solvent molecules such as dichloromethane, methanol, n-butanol or chloroform are complexed into the resorcinar…
Equipping metallo-supramolecular macrocycles with functional groups: Assemblies of pyridine-substituted urea ligands
A series of di-(m-pyridyl)-urea ligands were prepared and characterized with respect to their conformations by NOESY experiments and crystallography. Methyl substitution in different positions of the pyridine rings provides control over the position of the pyridine N atoms relative to the urea carbonyl group. The ligands were used to self-assemble metallo-supramolecular M(2)L(2) and M(3)L(3) macrocycles which are generated in a finely balanced equilibrium in DMSO and DMF according to DOSY NMR experiments and ESI FTICR mass spectrometry. Again, crystallography was used to characterize the assemblies. Methyl substitution in positions next to the pyridine nitrogen prevents coordination, while …
Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry.
A tris(bipyridine) ligand 1 with two BINOL (BINOL = 2, 2′-dihydroxy-1, 1′-binaphthyl) groups has been prepared in two enantiomerically pure forms. This ligand undergoes completely diastereoselective self-assembly into D2-symmeteric double-stranded trinuclear helicates upon coordination to copper(I) and silver(I) ions and to D3-symmetric triple-stranded trinuclear helicates upon coordination to copper(II), zinc(II), and iron(II) ions as demonstrated by mass spectrometry, NMR and CD spectroscopy in combination with quantum chemical calculations and X-ray diffraction analysis. According to the calculations, the single diastereomers that are formed during the self-assembly process are strongly …
[2,6-Bis(di-tert-butylphosphinomethyl)phenyl-κ3P,C1,P′](trifluoroacetato)palladium(II)
The Pd(II) atom in the title compound, [Pd(C(2)F(3)O(2))(C(24)H(43)P(2))], adopts a distorted square-planar geometry with the P atoms in a trans arrangement, forming two five-membered chelate rings. Four intra-molecular C-H⋯O hydrogen bonds occur. The crystal packing reveals one weak inter-molecular C-H⋯O hydrogen bond, which self-assembles the mol-ecules into infinite chains parallel to the b axis.
The new 5- or 6-azapyrimidine and cyanuric acid derivatives of L-ascorbic acid bearing the free C-5 hydroxy or C-4 amino group at the ethylenic spacer: CD-spectral absolute configuration determination and biological activity evaluations
Abstract We report on the synthesis of the novel types of cytosine and 5-azacytosine (1–9), uracil and 6-azauracil (13–18) and cyanuric acid (19–22) derivatives of l -ascorbic acid, and on their cytostatic activity evaluation in human malignant tumour cell lines vs. their cytotoxic effects on human normal fibroblasts (WI38). The CD spectra analysis revealed that cytosine (5 and 6), uracil (14–16), 6-azauracil (17) and cyanuric acid (21) derivatives of l -ascorbic acid bearing free amino group at ethylenic spacer existed as a racemic mixture of enantiomers, whereas L-ascorbic derivatives containing the C-5 substituted hydroxy group at the ethylenic spacer were obtained in (4R, 5S) enantiomer…
[2,6-Bis(di-tert-butylphosphinomethyl)phenyl-κ3P,C1,P′](trifluoroacetato)palladium(II)
The PdII atom in the title compound, [Pd(C2F3O2)(C24H43P2)], adopts a distorted square-planar geometry with the P atoms in a trans arrangement, forming two five-membered chelate rings. Four intramolecular C—H...O hydrogen bonds occur. The crystal packing reveals one weak intermolecular C—H...O hydrogen bond, which self-assembles the molecules into infinite chains parallel to the b axis.
Preparation of potentially porous, chiral organometallic materials through spontaneous resolution of pincer palladium conformers.
Understanding the mechanism by which advanced materials assemble is essential for the design of new materials with desired properties. Here, we report a method to form chiral, potentially porous materials through spontaneous resolution of conformers of a PCP pincer palladium complex ({2,6-bis[(di-t-butylphosphino)methyl]phenyl}palladium(II)halide). The crystallisation is controlled by weak hydrogen bonding giving rise to chiral qtz-nets and channel structures, as shown by 16 such crystal structures for X = Cl and Br with various solvents like pentane and bromobutane. The fourth ligand (in addition to the pincer ligand) on palladium plays a crucial role; the chloride and the bromide primaril…
Self-Complementary Dimers of Oxalamide-Functionalized Resorcinarene Tetrabenzoxazines
Self‐complementarity is a useful concept in supramolecular chemistry, molecular biology and polymeric systems. Two resorcinarene tetrabenzoxazines decorated with four oxalamide groups were synthesized and characterized. The oxalamide groups possessed self‐complementary hydrogen bonding sites between the carbonyls and amide groups. The self‐complementary nature of the oxalamide groups resulted in self‐included dimeric assemblies. The hydrogen bonding interactions within the tetrabenzoxazines gave rise to the formation of dimers, which were confirmed by single‐crystal X‐ray diffractions analysis and supported by NMR spectroscopy and mass spectrometry. The self‐included dimers were connected b…
Halogen-bonded solvates of tetrahaloethynyl cavitands
The formation and structures of halogen-bonded solvates of three different tetrahaloethynyl cavitands with acetone, chloroform, acetonitrile, DMF and DMSO were prepared and investigated. The inclusion and host–guest behaviour of the resorcinarene cavitands was found to be highly dependent on the flexibility of the ethylene-bridging unit.
C2-Symmetric Ferrocene-Bis(ureido)peptides : Synthesis, Conformation and Solid-State Structure
The extension of peptide derivatives of ferrocene-1,1'-dicarboxylic acid by formal insertion of NH units between ferrocene and peptide strands results in ferrocene-bis(ureido)-peptides. Experimentally, alanine and dialanine methyl esters were attached to the 1- and 1'-position of 1,1'-diiso-cyanoferrocene to give the corresponding bis(ureido)peptide derivatives 3 and 4. The conformation of 3 has been determined in the solid state by X-ray crystallography. In solution the preferred conformation of 3 and 4 has been elucidated by NMR, IR and CD spectroscopy in concert with DFT calculations. The secondary structure of ferrocene―bis(ureido)peptides 3 and 4 is determined by double bifurcated intr…
Counterion influence on the N–I–N halogen bond
A detailed investigation of the influence of counterions on the [N–I–N]+ halogen bond in solution, in the solid state and in silico is presented. Translational diffusion coefficients indicate close attachment of counterions to the cationic, three-center halogen bond in dichloromethane solution. Isotopic perturbation of equilibrium NMR studies performed on isotopologue mixtures of regioselectively deuterated and nondeuterated analogues of the model system showed that the counterion is incapable of altering the symmetry of the [N–I–N]+ halogen bond. This symmetry remains even in the presence of an unfavorable geometric restraint. A high preference for the symmetric geometry was found also in …
Binding Modes of Nonspherical Anions to N-Alkylammonium Resorcinarenes in the Solid State
A series of hydrogen bond stabilized N-alkylammonium resorcinarene salts with nitrate, triflate, and picrate as the counteranions were synthesized and characterized with 1H NMR and electrospray ionization (ESI) mass spectrometry. Together with electrostatic interactions, the binding of the anions with several hydrogen bond donor sites proceeds through a complex array of intra- and intermolecular hydrogen bonds, evidenced by single crystal X-ray diffraction analysis. These N-alkyl ammonium resorcinarenes bind the larger nonspherical anions into deformed cavitand-like structures and enforce a transformation of the resorcinarene conformation from almost symmetrical to extremely distorted.
Counterion influence on the N–I–N halogen bond† †Electronic supplementary information (ESI) available: Experimental details of synthesis, compound characterisation, IPE NMR measurements, computational and crystallographic procedures, and crystal data for 1-Ag/I to 7-Ag/I, and 12-Ag. CCDC 1045981–1045995. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc01053e Click here for additional data file. Click here for additional data file.
Counterions influence three-center halogen bonds differently than coordination bonds of transition metals.
CCDC 990706: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Altti Ala-Korpi, Mario Cetina, Arto Valkonen, Kari Rissanen|2014|Chem.-Eur.J.|20|15144|doi:10.1002/chem.201402533
CCDC 967821: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Mario Cetina, Kari Rissanen|2014|Chem.Commun.|50|1959|doi:10.1039/C3CC49010F
CCDC 1045987: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 913158: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 1045995: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 990709: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Altti Ala-Korpi, Mario Cetina, Arto Valkonen, Kari Rissanen|2014|Chem.-Eur.J.|20|15144|doi:10.1002/chem.201402533
CCDC 1045983: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 2060885: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 1045988: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 1577820: Experimental Crystal Structure Determination
Related Article: Zoran Džolić, Ngong Kodiah Beyeh, Mario Cetina, Lotta Turunen, Kari Rissanen|2018|Chem.Asian J.|13|164|doi:10.1002/asia.201701426
CCDC 2060891: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 1556027: Experimental Crystal Structure Determination
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1045990: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 2060888: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 955661: Experimental Crystal Structure Determination
Related Article: Julià Arcau, Vincent Andermark, Elisabet Aguiló, Albert Gandioso, Artur Moro, Mario Cetina, João Carlos Lima, Kari Rissanen, Ingo Ott, Laura Rodríguez|2014|Dalton Trans.|43|4426|doi:10.1039/C3DT52594E
CCDC 1577819: Experimental Crystal Structure Determination
Related Article: Zoran Džolić, Ngong Kodiah Beyeh, Mario Cetina, Lotta Turunen, Kari Rissanen|2018|Chem.Asian J.|13|164|doi:10.1002/asia.201701426
CCDC 2060887: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 1045984: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 1045981: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 829593: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Mario Cetina,Kari Rissanen|2012|Cryst.Growth Des.|12|4919|doi:10.1021/cg3008409
CCDC 913147: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 913151: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 1577818: Experimental Crystal Structure Determination
Related Article: Zoran Džolić, Ngong Kodiah Beyeh, Mario Cetina, Lotta Turunen, Kari Rissanen|2018|Chem.Asian J.|13|164|doi:10.1002/asia.201701426
CCDC 1556030: Experimental Crystal Structure Determination
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 913154: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 967819: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Mario Cetina, Kari Rissanen|2014|Chem.Commun.|50|1959|doi:10.1039/C3CC49010F
CCDC 927661: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 913161: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 990707: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Altti Ala-Korpi, Mario Cetina, Arto Valkonen, Kari Rissanen|2014|Chem.-Eur.J.|20|15144|doi:10.1002/chem.201402533
CCDC 1556033: Experimental Crystal Structure Determination
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 913150: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 913155: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 955660: Experimental Crystal Structure Determination
Related Article: Julià Arcau, Vincent Andermark, Elisabet Aguiló, Albert Gandioso, Artur Moro, Mario Cetina, João Carlos Lima, Kari Rissanen, Ingo Ott, Laura Rodríguez|2014|Dalton Trans.|43|4426|doi:10.1039/C3DT52594E
CCDC 990708: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Altti Ala-Korpi, Mario Cetina, Arto Valkonen, Kari Rissanen|2014|Chem.-Eur.J.|20|15144|doi:10.1002/chem.201402533
CCDC 913149: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 913148: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 990705: Experimental Crystal Structure Determination
Related Article: N. Kodiah Beyeh, Altti Ala-Korpi, Mario Cetina, Arto Valkonen, Kari Rissanen|2014|Chem.-Eur.J.|20|15144|doi:10.1002/chem.201402533
CCDC 1045982: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 913160: Experimental Crystal Structure Determination
Related Article: Magnus T. Johnson,Zoran Dolic,Mario Cetina,Manu Lahtinen,Marten S. G. Ahlquist,Kari Rissanen,Lars Ohrstrom,Ola F. Wendt|2013|Dalton Trans.|42|8484|doi:10.1039/c3dt50190f
CCDC 1045992: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 1556029: Experimental Crystal Structure Determination
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 2060884: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 2060886: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 2060892: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 1045991: Experimental Crystal Structure Determination
Related Article: Michele Bedin, Alavi Karim, Marcus Reitti, Anna-Carin C. Carlsson, Filip Topić, Mario Cetina, Fangfang Pan, Vaclav Havel, Fatima Al-Ameri, Vladimir Sindelar, Kari Rissanen, Jürgen Gräfenstein, Máté Erdélyi|2015|Chemical Science|6|3746|doi:10.1039/C5SC01053E
CCDC 1003004: Experimental Crystal Structure Determination
Related Article: Christoph Gütz , Rainer Hovorka , Niklas Struch , Jens Bunzen , Georg Meyer-Eppler , Zheng-Wang Qu , Stefan Grimme , Filip Topić, Kari Rissanen, Mario Cetina, Marianne Engeser, Arne Lützen|2014|J.Am.Chem.Soc.|136|11830|doi:10.1021/ja506327c
CCDC 2060893: Experimental Crystal Structure Determination
Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J
CCDC 1556032: Experimental Crystal Structure Determination
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CCDC 913159: Experimental Crystal Structure Determination
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