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Mark J MacLachlan

Publications and source records attributed to Mark J MacLachlan.

15 recordsLinked to original sources
PubMed2006

Heptametallic bowl-shaped complexes derived from conjugated Schiff-base macrocycles: synthesis, characterization, and X-ray crystal structures.

The reaction of chelating conjugated macrocycles 1a-c with Zn(OAc)2 gives bowl-shaped heptanuclear Zn complexes featuring Zn in tetrahedral, octahedral, and square-pyramidal geometries. Crystallographic and NMR results indicate that vacant Zn coordination sites within the bowl may be accessed, suggesting that these coordination complexes may be used as mimics for Zn fingers and carbonic anhydrase.

Journal Article↗
PubMed2006

[6 + 6] Schiff-base macrocycles with 12 imines: giant analogues of cyclohexane.

Hexagon-shaped [6 + 6] Schiff-base macrocycles with 12 imine bonds are reported. These giant macrocycles possess 6 N2O2 coordination environments and mass spectrometry evidence for hexametallation of one macrocycle is provided. Semi-empirical calculations reveal two stable conformations with boat and chair geometries for the macrocycles metallated with Ni(II), analogous to the conformations observed for cyclohexane.

Cyclohexanes↗
PubMed2006

Tetraalkoxyphenanthrene: a new precursor for luminescent conjugated polymers.

[reaction: see text] We have developed a convenient synthesis of tetraalkoxyphenanthrene derivatives and demonstrated their use to form luminescent conjugated oligomers and polymers. Palladium-catalyzed cross-coupling reactions of 2,7-diiodo-3,6-dimethoxy-9,10-di(2-ethylhexyloxy)phenanthrene produced high molecular weight poly(p-phenylene ethynylene)s and low molecular weight poly(p-phenylene vinylene)s. These new polymers, which are luminescent in the solid state and in solution, may be useful for developing LED or solar cell devices, or in chemical sensors.

Journal Article↗
PubMed2006

Robust non-interpenetrating coordination frameworks from new shape-persistent building blocks.

New shape-persistent ligands derived from triptycene were synthesized, and reaction with copper iodide results in the assembly of non-interpenetrating coordination frameworks with hydrophobic void spaces. These structures are thermally stable and display reversible solvent adsorption, and 1H NMR experiments show that they can be used to remove benzene from water.

Journal Article↗
PubMed2006

N-salicylideneanilines: tautomers for formation of hydrogen-bonded capsules, clefts, and chains.

[structure: see text] The synthesis, characterization, and solid-state structures of new salicylaldimines are reported. Bis(N-salicylideneaniline)s (BSANs) and tris(N-salicylideneaniline)s (TSANs) are sterically encumbered compounds featuring a central six-membered ring in the keto-enamine tautomer. When extended with additional functional groups, these molecules may form hydrogen-bonded capsules, clefts, and extended structures. A TSAN with N-(t)()BOC-o-phenylenediamine groups has been structurally investigated. The complementary hydrogen-bonding motif in this molecule leads it to form dimers in solution and in the solid state. A BSAN with N-(t)()BOC-o-phenylenediamine substituents forms a hydrogen-bonded cleft in solution but forms an extended hydrogen-bonded ladder assembly of cofacial dimers in the solid state. When N-(t)()BOC-1,8-naphthalenediamine was utilized to extend the cleft, an unusual perimidine structure was obtained with the central core in the enol tautomer. In addition, ab initio calculations have been used to support the assignment of the keto-enamine or enol-imine tautomers of the BSANs and TSANs and to predict tautomerization in related BSANs and TSANs.

Journal Article↗
PubMed2005

Tautomerization in naphthalenediimines: a keto-enamine Schiff base macrocycle.

[reaction: see text] A new [3 + 3] Schiff base macrocycle incorporating naphthalene groups has been prepared. By examination of its properties, X-ray crystallography of model compounds, and calculations, it has been determined that the macrocycle exists predominantly as the keto-enamine tautomer. This unexpected tautomerization presents an unusual hexaketo interior in the macrocycle.

Journal Article↗
PubMed2005

Synthesis, structure, and computational studies of soluble conjugated multidentate macrocycles.

[Chemical reaction: See text] Conjugated, shape-persistent macrocycles based on [3 + 3] Schiff-base condensation are of interest for supramolecular materials. In an effort to develop new discotic liquid crystals based on these compounds, a series of macrocycles with peripheral alkoxy groups of varying length have been prepared. The synthesis and mechanism of formation have been probed by isolation of oligomeric intermediates. A single-crystal X-ray diffraction study of one macrocycle revealed a nonplanar, strongly hydrogen-bonded structure. To our surprise, even with very long substituents, the macrocycles were not liquid crystalline. This has been rationalized by ab initio calculations that indicate the macrocycles are undergoing rotation of the dihydroxydiiminobenzene rings that may not allow a stable discotic liquid crystalline phase. These results provide new insight into the formation and properties of these large macrocycles and may provide guidance to developing stable liquid crystalline materials in the future.

Journal Article↗
PubMed2004

Mild and selective reduction of imines: formation of an unsymmetrical macrocycle.

During investigations of 5, a [3 + 3] Schiff-base macrocycle with six imines, a partially reduced Schiff-base macrocycle, 6, possessing one CH(2)NH and five imine groups was obtained. Control experiments and deuterium labeling indicate that the macrocycle is reduced by a benzimidazoline generated during the reaction. Benzimidazolines may be convenient reagents for the mild and selective reduction of imines.

Cyclization↗
PubMed2004

Synthesis and metalation of novel fluorescent conjugated macrocycles.

[reaction: see text] Large shape-persistent conjugated macrocycles with tunable pore diameters in the nanometer regime were prepared by a simple, one-pot procedure. These new self-assembled macrocycles contain rings of 48-66 covalently bonded atoms and can bind multiple metal ions, forming soluble luminescent complexes.

Journal Article↗
PubMed2004

Rotaxanated conjugated sensory polymers.

Two highly emissive conjugated polymers with tethered rotaxane repeat units are reported. Hydrogen bonding between acidic alcohols and the N-heteroaromatic groups in the rotaxanes attenuates polymer fluorescence. In addition, the rotaxane groups create precise three-dimensional pockets for metal binding, which results in fluorescence quenching. Exposing thin films of Zn-doped polymers to alcohol vapors reverses the quenching by up to 25%.

Journal Article↗
PubMed2003

Highly stable keto-enamine salicylideneanilines.

[reaction: see text] Highly stable NH salicylideneanilines have been prepared by reaction of 1,3,5-triformylphloroglucinol with aniline derivatives. The NH form was confirmed by X-ray crystallographic data, as well as by NMR studies. A convenient one-step synthesis of triformylphloroglucinol is also reported.

Journal Article↗
PubMed2003

Novel route to periodic mesoporous aminosilicas, PMAs: ammonolysis of periodic mesoporous organosilicas.

A new route to periodic mesoporous aminosilicas (PMAs) that contain amine functional groups in the framework of a mesoporous network is reported. The materials are prepared via thermal ammonolysis of periodic mesoporous organosilicas (PMOs) under a flow of ammonia gas. PMOs integrate similar or even higher quantities of nitrogen-containing groups upon ammonolysis than similarly treated ordered mesoporous silicas (MCM-41). The quantity of amine groups introduced into the materials was found to depend strongly on the ammonolysis temperature. The largest loading of amine groups was obtained when a well-ordered cubic methylene PMO material without prior vacuum-drying was thermolyzed in ammonia. The ordered mesoporosity of PMOs was preserved during the ammonolysis with only a slight decrease in the mesopore size and the degree of mesostructural ordering. The extent of substitution of framework oxygen by amine and nitride groups was established by solid-state (29)Si CP-MAS, (29)Si MAS, (15)N MAS, and (13)C CP-MAS NMR spectroscopies, elemental analysis, and X-ray photoelectron spectroscopy. In some cases, methylene and methyl functional groups were also present in the PMAs along with amine functional groups, as inferred from elemental analysis and gas adsorption, particularly in cases where PMOs were subjected to ammonolysis at 400 and 550 degrees C for several hours. This resulted in new multifunctional mesoporous organoaminosilica nanomaterials with properties that could be tuned by systematically varying the relative amounts of hydrophilic amine and hydrophobic hydrocarbon pendent and framework groups. The stability upon storage was found to be much higher for PMAs obtained from PMOs than for those obtained from MCM-41 silicas under the same conditions.

Journal Article↗
PubMed2002

Genesis of nanostructured, magnetically tunable ceramics from the pyrolysis of cross-linked polyferrocenylsilane networks and formation of shaped macroscopic objects and micron scale patterns by micromolding inside silicon wafers.

The ability to form molded or patterned metal-containing ceramics with tunable properties is desirable for many applications. In this paper we describe the evolution of a ceramic from a metal-containing polymer in which the variation of pyrolysis conditions facilitates control of ceramic structure and composition, influencing magnetic and mechanical properties. We have found that pyrolysis under nitrogen of a well-characterized cross-linked polyferrocenylsilane network derived from the ring-opening polymerization (ROP) of a spirocyclic [1]ferrocenophane precursor gives shaped macroscopic magnetic ceramics consisting of alpha-Fe nanoparticles embedded in a SiC/C/Si(3)N(4) matrix in greater than 90% yield up to 1000 degrees C. Variation of the pyrolysis temperature and time permitted control over the nucleation and growth of alpha-Fe particles, which ranged in size from around 15 to 700 A, and the crystallization of the surrounding matrix. The ceramics contained smaller alpha-Fe particles when prepared at temperatures lower than 900 degrees C and displayed superparamagnetic behavior, whereas the materials prepared at 1000 degrees C contained larger alpha-Fe particles and were ferromagnetic. This flexibility may be useful for particular materials applications. In addition, the composition of the ceramic was altered by changing the pyrolysis atmosphere to argon, which yielded ceramics that contain Fe(3)Si(5). The ceramics have been characterized by a combination of physical techniques, including powder X-ray diffraction, TEM, reflectance UV-vis/near-IR spectroscopy, elemental analysis, XPS, SQUID magnetometry, Mössbauer spectroscopy, nanoindentation, and SEM. Micromolding of the spirocyclic [1]ferrocenophane precursor within soft lithographically patterned channels housed inside silicon wafers followed by thermal ROP and pyrolysis enabled the formation of predetermined micron scale designs of the magnetic ceramic.

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