Coordination capabilities of a novel organic polychlorotriphenylmethyl monosulfonate radical

The treatment of alpha-H-p-H-PTM (PTM = polychlorotriphenylmethane) with oleum 65% followed by deprotonation and oxidation leads to the isolation of a novel pure organic radical PTMSO3H x 3 H2O x 0.5 hexane (2). The X-ray diffraction of 2 reveals a layered structure with disordered H2O molecules between facing sulfonic acid groups. We have explored the coordination abilities of the sulfonate derivative using different metals. The treatment of 2 with mild bases yields the sulfonate radical PTMSO3Na x H2O (3). On the other hand, the new compound [Cu(py)2(H2O)4](PTMSO3)2 x 2 H2O x 2 EtOH (4) has been crystallized using Cu(II) as the metallic counterion in the presence of pyridine. The structure reveals a solvent-separated ion-pair-type compound, with no direct coordination of the metal ion with the sulfonate group, and the formation of organic layers between layers of transition metal complexes. This situation has been overcome by favoring the stabilization of the sulfonate group over the Cu(II) center by changing the pyridine ligand to cyclam. This has led to compound [Cu(cyclam)](PTMSO3)2 x 6 EtOH (5a), in which the sulfonate group acts as a monodentate axial ligand for the Cu(II) center. We have observed a single-to-single crystal rearrangement from 5a to [Cu(cyclam)](PTMSO3)2 (5b) because of the loss of the solvent of crystallization, without significant modification of the metal coordination environment. All species have been structurally and magnetically characterized, and the magnetic coupling between the organic radicals and the metal paramagnetic centers is discussed.     

Specific solvent effects on the intramolecular electron transfer reaction in a neutral ferrocene donor polychlorotriphenylmethyl acceptor radical with extended conjugation

The synthesis and the optical, magnetic and electrochemical properties of the ferrocenylbutynene substituted polychlorotriphenylmethyl radical 1 are reported. Radical 1 is prepared in a three step synthetic route starting with a Wittig reaction to yield (E,Z)-{4-[4-(bis(2,3,4,5,6-pentachlorophenyl)methyl)-2,3,5,6-tetra-chlorophenyl]but-3-en-1-ynyl}-ferrocene (1H) which is subsequently deprotonated to yield the corresponding anion K⁺(18-crown-6) [1]^? and finally oxidized to (E)-4-[4-(ferrocenyl)but-3-yn-1-enyl]-2,3,5,6-tetrachlorophenyl-bis(2,3,4,5,6-pentachlorophenyl) methyl radical (1). Radical 1 exhibits a charge-transfer band transition in the near infrared region which is associated with an intramolecular electron transfer from the ferrocene unit (donor) to the radical unit (acceptor) of this dyad molecule; its solvatochromism is studied in detail. The X-ray crystal structure of [K⁺(18-crown-6)](E)-[4-[4-(ferrocenyl)but-3-yn-1-enyl]-2,3,5,6-tetrachlorophenyl-bis(2,3,4,5,6-pentachlorophenyl) methide] [1]^? has been determined. This organic salt forms an interesting one-dimensional coordination polymer by the coordination of the K⁺ cation with chlorine atoms of the organic carbanion.     

Stereochemistry and EPR investigation of a chiral molecular magnet

An electron paramagnetic resonance investigation of an indexed single crystal of the chiral molecular magnet (R)-3MLNN·Mn(hfac)₂ which is comprised of a chiral phenyl α-nitronyl nitroxide and a manganese(II) ion is presented. The crystal of the compound, which consists of ferrimagnetic chains of radical and metal ion and orders ferromagnetically below 4 K, shows temperature and angle-dependent spectra which may give clues as to the nature of the anisotropy in the system and the types of interaction at play.     

Spontaneous resolution and absolute configuration of a coordination polymer formed by MnII and a ferrocene-based bisnitronyl nitroxide radical

Crystallisation of a ferrocenyl bis(nitronyl nitroxide) with manganese(II) bis(hexafluoroacetylacetonate) gives rise to spontaneous resolution of a coordination polymer formed by the two units creating seven sources of chirality.     

Synthesis,separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative

The synthesis, isolation and STM imaging on graphite of the cis and trans isomers of a TTF reveal isomer-dependent packing, and constitutes a way to study the non-covalent interactions at play in these systems.     

Synthesis, Characterization, and Theoretical Study of Sulfur-Containing Donor-Acceptor DCNQI Derivatives with Photoinduced Intramolecular Electron Transfer

The donor-acceptor compounds N,N'-dicyanobenzo[b]naphtho[2,3-e][1,4]dithiin-6,11-quinonediimine (9a) and N,N'-dicyanobenzo[b]naphtho[2,3-e][1,4]oxathiin-6,11-quinonediimine (10a) and their methyl-substituted derivatives (9b and 10b-d, respectively) have been prepared, and their structural and electronic properties have been characterized by both experimental techniques and quantum-chemical calculations. The (1)H-NMR spectra evidence the existence of a syn/anti isomerism in solution. Both experimental and theoretical data suggest that the preferred configuration of the N-CN groups corresponds to a syn isomer for 9 and to an anti isomer for 10. The X-ray analysis performed for 9b reveals that molecules are not planar and pack in vertical stacks showing an overlap between donor and acceptor moieties of adjacent molecules. In agreement with X-ray data, theoretical calculations predict that both for 9 and 10 the acceptor DCNQI moiety is folded and adopts a butterfly-type structure and the donor moiety is bent along the line passing through the heteroatoms. The energy difference between planar and butterfly structures is calculated to be < 3 kcal/mol at the ab initio 6-31G level. The UV-vis spectra present a broad absorption in the visible which corresponds to a photoinduced intramolecular electron transfer from the high-energy HOMO furnished by the donor moiety to the low-energy LUMO located on the DCNQI fragment. Cyclic voltammetry displays one oxidation peak to the cation and two one-electron reduction waves to the anion and dianion. Theoretical calculations show the planarization of the acceptor/donor moiety induced by reduction/oxidation. The formation of stable radical anions is corroborated by the intense EPR signals recorded for reduced 9. The assignment of the hyperfine coupling constants of the EPR spectra is consistent with the existence of a preferred syn configuration.