Ognjen S. Miljanic

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Name: Miljanic, Ognjen; Ognjen Š. Miljanić
Organization: University of Houston , USA
Department: Department of Chemistry
Title: Associate(PhD)

TOPICS

Co-reporter:Zhenglin Zhang;Mohamed I. Hashim;Ognjen Š. Miljanić
Chemical Communications 2017 vol. 53(Issue 72) pp:10022-10025
Publication Date(Web):2017/09/05
DOI:10.1039/C7CC03814C
Trigonal fluorinated pyrazoles assemble into porous molecular crystals and show solid-state fluorescence. However, in a DMF/H2O mixed solvent system, the triazine-centered compound displays aggregation-induced emission, while its benzene-based counterpart does not.
Co-reporter: Teng-Hao Chen;Dr. Ilya Popov; Ognjen Š. Miljanić
Chemistry - A European Journal 2017 Volume 23(Issue 2) pp:286-290
Publication Date(Web):2017/01/05
DOI:10.1002/chem.201605079
AbstractA microporous metal–organic framework (MOF) was synthesized from [Zr6O4(OH)4(C6H5COO)12] clusters and a triacid ligand based on a shape-persistent arylene ethynylene macrocycle. This framework, dubbed Zr-MCMOF, is held together by metal–ligand coordination and multiple weak interactions: hydrogen bonding, [π⋅⋅⋅π] stacking, and [C−H⋅⋅⋅π] interactions. The rigid ligand has a 9 Å-wide central void, which serves as a predesigned aperture for the 1D channels; all of the porosity of Zr-MCMOF comes from the ligand. The resulting framework possesses high hydrolytic and thermal stability and a flexible structure unique among Zr-based MOFs.
Co-reporter:Ognjen Š. Miljanić
Chem 2017 Volume 2, Issue 4(Volume 2, Issue 4) pp:
Publication Date(Web):13 April 2017
DOI:10.1016/j.chempr.2017.03.002
Some of the key scientific advances of the past century—nuclear energy, artificial fertilizers, or vaccines—came from the domain of a single discipline: physics, chemistry, or biology. As the 21st century unfolds, it is increasingly clear that the pressing problems in energy, climate, and medicine will not be solved in the same way. Instead, they will need close cooperation of the traditional branches of science. Such collaborative ventures will necessitate understanding of complex systems in their entirety and will build on the reductionist understanding of a system's individual components. Key insights from this systems-level approach will be related to the interactions between actors in a complex unity, emergent properties observable only within a system rather than assigned to individual actors, and the phenomena that occur across different length scales. Systems chemistry aims to retool the traditional understanding of chemical phenomena to be better suited to these global challenges.Systems chemistry is a broad and relatively new approach to studying chemical phenomena by embracing and understanding their inherent complexity rather than seeking to limit or eliminate it. Systems-level understanding is a powerful alternative to the traditionally reductionist approach that many branches of chemistry currently utilize. Complex chemical systems can operate under kinetic or thermodynamic control and give rise to unique properties, some of which are emergent—that is, impossible to observe in individual components of the system. This review highlights selected examples of how the systems chemistry approach has been used for studying dynamic combinatorial libraries, autocatalytic processes, chemical reactions at the origins of life, as well as for reaction discovery and synthesis of complex functional molecules, including molecular machines.Download high-res image (374KB)Download full-size image
Co-reporter:Christopher H. Hendon, Kate E. Wittering, Teng-Hao Chen, Watchareeya Kaveevivitchai, Ilya Popov, Keith T. Butler, Chick C. Wilson, Dyanne L. Cruickshank, Ognjen Š. Miljanić, and Aron Walsh
Nano Letters 2015 Volume 15(Issue 3) pp:2149-2154
Publication Date(Web):February 23, 2015
DOI:10.1021/acs.nanolett.5b00144
Atmospherically stable porous frameworks and materials are interesting for heterogeneous solid–gas applications. One motivation is the direct and selective uptake of pollutant/hazardous gases, where the material produces a measurable response in the presence of the analyte. In this report, we present a combined experimental and theoretical rationalization for the piezochromic response of a robust and porous molecular crystal built from an extensively fluorinated trispyrazole. The electronic response of the material is directly determined by analyte uptake, which provokes a subtle lattice contraction and an observable bathochromic shift in the optical absorption onset. Selectivity for fluorinated absorbates is demonstrated, and toluene is also found to crystallize within the pore. Furthermore, we demonstrate the application of electronic structure calculations to predict a physicochemical response, providing the foundations for the design of electronically tunable porous solids with the chemical properties required for development of novel gas-uptake media.
Co-reporter:Teng-Hao Chen, Watchareeya Kaveevivitchai, Allan J. Jacobson and Ognjen Š. Miljanić  
Chemical Communications 2015 vol. 51(Issue 74) pp:14096-14098
Publication Date(Web):04 Aug 2015
DOI:10.1039/C5CC04885K
Commonly used inhalation anesthetics—enflurane, isoflurane, sevoflurane, halothane, and methoxyflurane—are adsorbed within the pores of a porous fluorinated molecular crystal to the tune of up to 73.4(±0.2)% by weight. Uptake of all studied anesthetics is quite fast, typically reaching saturation in less than three minutes.
Co-reporter:Teng-Hao Chen, Ilya Popov, Yu-Chun Chuang, Yu-Sheng Chen and Ognjen Š. Miljanić  
Chemical Communications 2015 vol. 51(Issue 29) pp:6340-6342
Publication Date(Web):04 Mar 2015
DOI:10.1039/C5CC01635E
A mesoporous Zn-based metal–organic framework (MOF) was prepared from a shape-persistent phenylene ethynylene macrocycle functionalized with three –COOH groups. The rigid ligand has a ∼9 Å wide central cavity which serves as a predesigned pore. The macrocycles [π⋯π] stack into pairs, with their carboxylate groups connected via three Zn3O14C6H2 clusters. The resulting MOF has a void volume of 86%.
Co-reporter:Merry K. Smith and Ognjen Š. Miljanić  
Organic & Biomolecular Chemistry 2015 vol. 13(Issue 29) pp:7841-7845
Publication Date(Web):25 Jun 2015
DOI:10.1039/C5OB01101A
Supramolecular chemistry of conjugated and conformationally rigid arylene ethynylene macrocycles (AEMs) has been the subject of increasing recent interest. AEMs are suited to function as supramolecular building blocks and hosts for small molecular guests thanks to their well-defined, non-collapsible central cavities and the potential for long range ordering through intermolecular π-stacking. Their syntheses are highly modular—albeit typically lengthy—allowing access to a great structural variety of AEM candidates for applications as carbon-rich mesogens and ligands in liquid crystals, nanoporous solids, molecular electronics, and chemical sensors. In this perspective, we highlight our recent work on the inclusion complexes and porous materials constructed from AEMs. Through this prism, we reflect on the recent advances and the remaining challenges in the supramolecular chemistry of AEMs.
Co-reporter:Ha T. M. Le, Nadia S. El-Hamdi, and Ognjen Š. Miljanić
The Journal of Organic Chemistry 2015 Volume 80(Issue 10) pp:5210-5217
Publication Date(Web):April 27, 2015
DOI:10.1021/acs.joc.5b00616
A series of 11 cross-conjugated cruciform fluorophores based on a benzobisimidazole nucleus has been synthesized and characterized. Like in their previously reported benzobisoxazole counterparts, the HOMOs of these new fluorophores are localized along the vertical bisethynylbenzene axes, while their LUMOs remain relatively delocalized across the molecule, except in cruciforms substituted with electron-withdrawing groups along the vertical axis. Benzobisimidazole cruciforms exhibit a pronounced response to deprotonation in their UV/vis absorption and emission spectra, but their response to protonation is significantly attenuated.
Co-reporter:Dr. Ilya Popov;Dr. Teng-Hao Chen;Dr. Sergey Belyakov; Olafs Daugulis; Steven E. Wheeler; Ognjen &x160;. Miljani&x107;
Chemistry - A European Journal 2015 Volume 21( Issue 7) pp:
Publication Date(Web):
DOI:10.1002/chem.201590028
Co-reporter:Chia-Wei Hsu ; Ognjen &x160;. Miljani&x107;
Angewandte Chemie 2015 Volume 127( Issue 7) pp:2247-2250
Publication Date(Web):
DOI:10.1002/ange.201409741

Abstract

Differences in adsorption among the components of complex mixtures play a role in separations, surface-based sensing, and heterogeneous catalysis, and have been implicated in theories of the origin of life. Herein, we consider mixtures of imines and we show that if such complex mixtures are also dynamic—that is, if their components equilibrate among themselves—then they can dramatically simplify in composition during the course of column chromatography. As they travel down the column, imines continuously trade their aldehyde and amine constituents, favoring the formation of molecules with extremes of polarity at the expense of species with intermediate polarities. Iterative application of this principle leads to simplification of imine libraries containing up to 16 members into 4 major products.

Co-reporter:Dr. Teng-Hao Chen;Dr. Ilya Popov;Dr. Watchareeya Kaveevivitchai;Dr. Yu-Chun Chuang;Dr. Yu-Sheng Chen; Allan J. Jacobson; Ognjen &x160;. Miljani&x107;
Angewandte Chemie 2015 Volume 127( Issue 47) pp:14108-14112
Publication Date(Web):
DOI:10.1002/ange.201505149

Abstract

Two mesoporous fluorinated metal–organic frameworks (MOFs) were synthesized from extensively fluorinated tritopic carboxylate- and tetrazolate-based ligands. The tetrazolate-based framework MOFF-5 has an accessible surface area of 2445 m2 g−1, the highest among fluorinated MOFs. Crystals of MOFF-5 adsorb hydrocarbons, fluorocarbons, and chlorofluorocarbons (CFCs)—the latter two being ozone-depleting substances and potent greenhouse species—with weight capacities of up to 225 %. The material exhibits an apparent preference for the adsorption of non-spherical molecules, binding unusually low amounts of both tetrafluoromethane and sulfur hexafluoride.

Co-reporter:Dr. Teng-Hao Chen;Dr. Ilya Popov;Dr. Watchareeya Kaveevivitchai;Dr. Yu-Chun Chuang;Dr. Yu-Sheng Chen; Allan J. Jacobson; Ognjen &x160;. Miljani&x107;
Angewandte Chemie International Edition 2015 Volume 54( Issue 47) pp:13902-13906
Publication Date(Web):
DOI:10.1002/anie.201505149

Abstract

Two mesoporous fluorinated metal–organic frameworks (MOFs) were synthesized from extensively fluorinated tritopic carboxylate- and tetrazolate-based ligands. The tetrazolate-based framework MOFF-5 has an accessible surface area of 2445 m2 g−1, the highest among fluorinated MOFs. Crystals of MOFF-5 adsorb hydrocarbons, fluorocarbons, and chlorofluorocarbons (CFCs)—the latter two being ozone-depleting substances and potent greenhouse species—with weight capacities of up to 225 %. The material exhibits an apparent preference for the adsorption of non-spherical molecules, binding unusually low amounts of both tetrafluoromethane and sulfur hexafluoride.

Co-reporter:Chia-Wei Hsu ; Ognjen &x160;. Miljani&x107;
Angewandte Chemie International Edition 2015 Volume 54( Issue 7) pp:2219-2222
Publication Date(Web):
DOI:10.1002/anie.201409741

Abstract

Differences in adsorption among the components of complex mixtures play a role in separations, surface-based sensing, and heterogeneous catalysis, and have been implicated in theories of the origin of life. Herein, we consider mixtures of imines and we show that if such complex mixtures are also dynamic—that is, if their components equilibrate among themselves—then they can dramatically simplify in composition during the course of column chromatography. As they travel down the column, imines continuously trade their aldehyde and amine constituents, favoring the formation of molecules with extremes of polarity at the expense of species with intermediate polarities. Iterative application of this principle leads to simplification of imine libraries containing up to 16 members into 4 major products.

Co-reporter:Dr. Ilya Popov;Dr. Teng-Hao Chen;Dr. Sergey Belyakov; Olafs Daugulis; Steven E. Wheeler; Ognjen &x160;. Miljani&x107;
Chemistry - A European Journal 2015 Volume 21( Issue 7) pp:2750-2754
Publication Date(Web):
DOI:10.1002/chem.201406073

Abstract

We report structural characterization of a new member of m-phenylene ethynylene ring family. This shape-persistent macrocycle also co-crystallizes with hexafluoro-, 1,2,4,5-tetrafluoro-, 1,3,5-trifluoro, and 1,4-difluorobenzene. The four complexes are almost isostructural, and all show the fluoroarene included into the central cavity of the macrocycle. Characterized by multiple short CH⋅⋅⋅FC contacts, these inclusion complexes further dimerize in the solid state into a 2+2 assembly, in which the two macrocycles embrace each other by their large hydrophobic groups that are rotated by 60° relative to one another.

Co-reporter:Qing Ji;Ha T. M. Le;Dr. Xiqu Wang;Dr. Yu-Sheng Chen;Dr. Tatyana Makarenko; Allan J. Jacobson; Ognjen &x160;. Miljani&x107;
Chemistry - A European Journal 2015 Volume 21( Issue 48) pp:17205-17209
Publication Date(Web):
DOI:10.1002/chem.201503851

Abstract

Cyanide-catalyzed benzoin condensation of terephthaldehyde produces a cyclic tetramer, which we propose to name cyclotetrabenzoin. Cyclotetrabenzoin is a square-shaped macrocycle ornamented with four α-hydroxyketone functionalities pointing away from the central cavity, the dimensions of which are 6.9×6.9 Å. In the solid state, these functional groups extensively hydrogen bond, resulting in a microporous three-dimensional organic framework with one-dimensional nanotube channels. This material exhibits permanent—albeit low-porosity, with a Langmuir surface area of 52 m2 g−1. Cyclotetrabenzoin’s easy and inexpensive synthesis and purification may inspire the creation of other shape-persistent macrocycles and porous molecular crystals by benzoin condensation.

Co-reporter:Qing Ji, Rio Carlo Lirag and Ognjen Š. Miljanić  
Chemical Society Reviews 2014 vol. 43(Issue 6) pp:1873-1884
Publication Date(Web):21 Jan 2014
DOI:10.1039/C3CS60356C
Dynamic combinatorial libraries (DCLs) are collections of structurally related compounds that can interconvert through reversible chemical reaction(s). Such reversibility endows DCLs with adaptability to external stimuli, as rapid interconversion allows quick expression of those DCL components which best respond to the disturbing stimulus. This Tutorial Review focuses on the kinetically controlled phenomena that occur within DCLs. Specifically, it will describe dynamic chiral resolution of DCLs, their self-sorting under the influence of irreversible chemical and physical stimuli, and the autocatalytic behaviours within DCLs which can result in self-replicating systems. A brief discussion of precipitation-induced phenomena will follow and the review will conclude with the presentation of covalent organic frameworks (COFs)—porous materials whose synthesis critically depends on the fine tuning of the crystal growth and error correction rates within large DCLs.
Co-reporter:Musabbir A. Saeed, Ha T. M. Le, and Ognjen Š. Miljanić
Accounts of Chemical Research 2014 Volume 47(Issue 7) pp:2074-2083
Publication Date(Web):April 29, 2014
DOI:10.1021/ar500099z
We have recently expanded our studies to benzimidazole-based “half-cruciforms”, which are L-shaped rigid fluorophores that maintain most of the spatial separation of FMOs observed in benzobisoxazole cruciforms. Unlike benzobisoxazoles, benzimidazoles are acidic on account of their polar N–H bonds, and this feature allows them to respond to a broader range of pH values than their benzobisoxazole counterparts. The deprotonated benzimidazolate anions maintain their fluorescence, which makes them promising candidates for incorporation into solid-state sensing materials known as zeolithic imidazolate frameworks.
Co-reporter:Teng-Hao Chen, Ilya Popov, Watchareeya Kaveevivitchai, and Ognjen Š. Miljanić
Chemistry of Materials 2014 Volume 26(Issue 15) pp:4322
Publication Date(Web):June 2, 2014
DOI:10.1021/cm501657d
Metal–organic frameworks (MOFs) are modular porous materials synthesized from metal cluster nodes and organic linkers that connect these nodes. This rapidly expanding class of structures presents viable platforms for applications in gas sorption and separation, catalysis, sensing, fuel processing, and environmental remediation and as porous conductive materials. These applications are increasingly relying on sophisticated ligands that have functional characteristics either as independent entities (that is, outside of MOFs) or that gain new functions once reticulated into the porous material. Thus, the traditionally inorganic area of MOF research begins to profit more and more from a comprehensive approach which combines insights from organic, inorganic, and materials chemistry. This Perspective highlights some of the second-generation MOFs prepared and studied using this holistic approach.
Co-reporter:Rio Carlo Lirag and Ognjen Š. Miljanić  
Chemical Communications 2014 vol. 50(Issue 66) pp:9401-9404
Publication Date(Web):01 Jul 2014
DOI:10.1039/C4CC02990A
Four acid-catalysed dehydration reactions can proceed in one pot, simultaneously and without interference, to yield one imine, one acetal (or boronic ester), one ester and one alkene, even though many other cross-products could be conceived. This advanced self-sorting behaviour is attributed to different dehydration rates, brought about by dissimilar electronic properties of starting materials.
Co-reporter:Qing Ji, Nadia S. El-Hamdi, and Ognjen Š. Miljanić
Journal of Chemical Education 2014 Volume 91(Issue 6) pp:830-833
Publication Date(Web):March 27, 2014
DOI:10.1021/ed400681w
Esters are volatile and pleasantly smelling compounds, commonly used as food additives. Using Ti(OBu)4-catalyzed acyl exchange, we demonstrate a scent transmutation experiment, in which two fragrant esters swap their acyl and alkoxy substituents and are, during the course of a reactive distillation, quantitatively converted into two different esters with distinct fragrance properties. We view this simple and appealing experiment as highly suitable for instructional use, since it can be used to teach the concepts of chemical equilibrium, distillation, transesterification, dynamic combinatorial chemistry, and the industrially relevant process of reactive distillation.Keywords: Chemical Engineering; Equilibrium; Esters; Gas Chromatography; Hands-On Learning/Manipulatives; Laboratory Instruction; NMR Spectroscopy; Organic Chemistry; Physical Chemistry; Upper-Division Undergraduate;
Co-reporter:Rio Carlo Lirag, Ha T. M. Le and Ognjen Š. Miljanić  
Chemical Communications 2013 vol. 49(Issue 39) pp:4304-4306
Publication Date(Web):18 Oct 2012
DOI:10.1039/C2CC37120K
Nine L-shaped benzimidazole fluorophores have been synthesized, computationally evaluated and spectroscopically characterized. These “half-cruciform” fluorophores respond to bases, acids and anions through changes in fluorescence that vary from moderate to dramatic.
Co-reporter:Teng-Hao Chen, Ilya Popov, Oussama Zenasni, Olafs Daugulis and Ognjen Š. Miljanić  
Chemical Communications 2013 vol. 49(Issue 61) pp:6846-6848
Publication Date(Web):07 Jun 2013
DOI:10.1039/C3CC41564C
Three perfluorinated Cu-based metal–organic frameworks (MOFs) were prepared starting from extensively fluorinated biphenyl-based ligands accessed via C–H functionalization. These new materials are highly hydrophobic: with water contact angles of up to 151 ± 1°, they are among the most water-repellent MOFs ever reported.
Co-reporter:Minyoung Jo, Jaebum Lim, and Ognjen Š. Miljanić
Organic Letters 2013 Volume 15(Issue 14) pp:3518-3521
Publication Date(Web):July 9, 2013
DOI:10.1021/ol401120a
Desilylation of silylethynyl-substituted benzobisoxazole cruciforms can be achieved using stoichiometric amounts of fluoride, leading to a significant change in their UV–vis absorption and fluorescence. This response is observable at micromolar concentrations of fluoride, and, in the case of a triisopropylsilyl-substituted cruciform fluorophore, extraordinarily selective for fluoride over other small inorganic anions, including hydroxide, acetate, and phosphate.
Co-reporter:Virginia Martínez-Martínez, Jaebum Lim, Jorge Bañuelos, Iñigo López-Arbeloa and Ognjen Š. Miljanić  
Physical Chemistry Chemical Physics 2013 vol. 15(Issue 41) pp:18023-18029
Publication Date(Web):23 Sep 2013
DOI:10.1039/C3CP53527D
A photophysical study was carried out on a series of nine X-shaped cross-conjugated compounds based on the benzobisoxazole nucleus. These “molecular cruciforms” were terminally substituted with electron-rich 4-(N,N-dimethylamino)phenyl, electron-neutral phenyl or electron-poor 4-pyridyl groups. Intramolecular charge transfer (ICT) transitions in molecular cruciforms were shown to be activated to a different extent by the combinations of these substituents located in different positions along vertical and/or horizontal axes of the molecules, showing strong emission throughout the visible spectrum. The high fluorescence efficiency and bathochromic shifts associated with the increasing polarity of the solvent make these cruciforms interesting candidates for use as fluorescence polarity indicators operating in a broad solvatochromic range.
Co-reporter:Qing Ji and Ognjen Š. Miljanić
The Journal of Organic Chemistry 2013 Volume 78(Issue 24) pp:12710-12716
Publication Date(Web):November 18, 2013
DOI:10.1021/jo402305p
Metal alkoxides, such as NaOt-Bu or Ti(OBu)4, can initiate acyl exchange within complex ester libraries. Reactive distillation of such dynamic combinatorial libraries (DCLs) isolates the most volatile ester at the expense of the less volatile library members that share a constituent with it. This process can be iteratively repeated to yield up to four industrially relevant esters as pure products from a single reaction setup. An algorithm has been developed to predict reactive distillation products in DCLs of as many as 121 members.
Co-reporter:Jaebum Lim, Dolly Nam and Ognjen Š. Miljanić  
Chemical Science 2012 vol. 3(Issue 2) pp:559-563
Publication Date(Web):17 Nov 2011
DOI:10.1039/C1SC00610J
The fluorescence of a single donor–acceptor benzobisoxazole-based cruciform, dissolved in five different solvents, dramatically changes upon exposure to Brønsted and Lewis acids. The changes in emission colors strongly depend on the analyte's structure, and this cruciform can discern among structurally closely related carboxylic (twelve examples) and organoboronic acids (nine examples). In combination with two commercially available phenylboronic acids, this cruciform sensor also distinguishes among substituted phenols (twelve examples).
Co-reporter:Jaebum Lim and Ognjen Š. Miljanić  
Chemical Communications 2012 vol. 48(Issue 83) pp:10301-10303
Publication Date(Web):03 Sep 2012
DOI:10.1039/C2CC35626K
A benzobisoxazole-based cruciform fluorophore forms fluorescent complexes with simple boronic acids. Through the changes of their fluorescence emission colours, these complexes can sense and qualitatively distinguish among structurally similar organic nitrogen compounds (amines and ureas) and small organic and inorganic anions. Preliminary results suggest that the intensity of this hybrid sensor's fluorescent response to chloride anions can be quantitatively correlated to chloride concentration.
Co-reporter:Teng-Hao Chen, Watchareeya Kaveevivitchai, Nghia Bui and Ognjen Š. Miljanić  
Chemical Communications 2012 vol. 48(Issue 23) pp:2855-2857
Publication Date(Web):18 Jan 2012
DOI:10.1039/C2CC17744G
Mild solvothermal dehydration of 1,1′-ferrocenediboronic acid produces a triply ferrocene-bridged boroxine cyclophane. Its crystal structure reveals a rigid trigonal prism that presents a minimal boroxine-based covalent organic polyhedron (COP).
Co-reporter:Jaebum Lim, Karolina Osowska, Jacob A. Armitage, Benjamin R. Martin and Ognjen Š. Miljanić  
CrystEngComm 2012 vol. 14(Issue 19) pp:6152-6162
Publication Date(Web):17 May 2012
DOI:10.1039/C2CE25485A
This paper explores the structural patterns adopted by a class of eight conjugated cruciforms based on a benzo[1,2-d:4,5-d′]bisoxazole (BBO) nucleus. Within the series, the lengths of cruciforms' x- and y-axes, as well as their terminal substituents, were varied. Two new cruciforms have been prepared using microwave-assisted Sonogashira couplings. Examination of molecular structures of BBO cruciforms revealed the expected cross-shaped geometries, with ∼90° crossing angles between the two conjugation circuits. Most significant deviations from the idealized planar structures were caused by the distortion of benzene rings positioned along the cruciforms' y-axis from the plane of the central benzobisoxazole ring, by as much as 82.1°. Deviations from linearity within carbon–carbon triple bonds were mild, but additively resulted in notably bent y-axes of the two largest examined cruciforms. Most significantly, the packing patterns of benzobisoxazole cruciforms revealed three distinct organizational motifs. Cruciforms with carbonyl groups on either the horizontal or the vertical axis (or both) all organized into two-dimensional infinite sheets, apparently connected chiefly through [C–H⋯O] contacts that varied in length between 2.24 and 2.60 Å, and could be interpreted as weak hydrogen bonds. The parallel layers of these two-dimensional sheets then assembled into three-dimensional structures through [π⋯π] stacking between the layers. The packing patterns of the two cruciforms with 4-(N,N-dimethylamino)phenyl groups on the vertical axis are dominated by one-dimensional columnar or tape-like assemblies that are formed through [π⋯π] stacking; these then organize into two-dimensional sheets, which in turn layer into a three-dimensional structure, but with a ∼60° angle between the adjacent sheets. Finally, in the parent tetraphenyl-substituted cruciform, the sp2 nitrogen on the BBO core plays the key role in the assembly. It establishes 2.64 Å-long [C–H⋯N] contacts with the phenyl groups, mediating the formation of a unique packing pattern in which six tilted columnar assemblies of [π⋯π] stacked cruciforms surround a three-fold rotation axis in the crystal.
Co-reporter:Rio Carlo Lirag, Karolina Osowska and Ognjen Š. Miljanić  
Organic & Biomolecular Chemistry 2012 vol. 10(Issue 25) pp:4847-4850
Publication Date(Web):21 May 2012
DOI:10.1039/C2OB25736J
Judicious choice of precipitation conditions can lead to self-sorting of equilibrating mixtures of aromatic aldehydes and substituted anilines into a handful of imine products. The selectivity of this process is caused by the solubility differences among possible imines in the EtOH–H2O solvent mixtures used in precipitation.
Co-reporter:Jaebum Lim and Ognjen Š. Miljanić  
CrystEngComm 2011 vol. 13(Issue 17) pp:5309-5312
Publication Date(Web):18 Jul 2011
DOI:10.1039/C1CE05618B
Crystal structures of two 8-arylethynyl substituted guanosines reveal twisted hydrogen-bonded ribbon superstructures, contrasting a previous report of guanine quartet formation from 8-aryl derivatives. The structural switch is attributed to the stabilization of the ribbon through intermolecular [π⋯π] stacking between the optimally positioned electron-poor arylethynyl substituents and electron-rich guanine nuclei.
Co-reporter:Dr. Karolina Osowska ; Ognjen &x160;. Miljani&x107;
Angewandte Chemie 2011 Volume 123( Issue 36) pp:8495-8499
Publication Date(Web):
DOI:10.1002/ange.201102813
Co-reporter:Dr. Karolina Osowska ; Ognjen &x160;. Miljani&x107;
Angewandte Chemie International Edition 2011 Volume 50( Issue 36) pp:8345-8349
Publication Date(Web):
DOI:10.1002/anie.201102813
Co-reporter:Jaebum Lim, Thomas A. Albright, Benjamin R. Martin, and Ognjen Š. Miljanić
The Journal of Organic Chemistry 2011 Volume 76(Issue 24) pp:10207-10219
Publication Date(Web):November 11, 2011
DOI:10.1021/jo202107w
We report the synthesis of nine conjugated cruciform-shaped molecules based on the central benzo[1,2-d:4,5-d′]bisoxazole nucleus, at which two conjugated currents intersect at a ∼90° angle. Cruciforms’ substituents were varied pairwise among the electron-neutral phenyl groups, electron-rich 4-(N,N-dimethylamino)phenyl substituents, and electron-poor pyridines. Hybrid density functional theory calculations revealed that the highest occupied molecular orbitals (HOMOs) are localized (24–99%) in all cruciforms, in contrast to the lowest unoccupied molecular orbitals (LUMOs) which are strongly dependent on the substitution and less localized (6–64%). Localization of frontier molecular orbitals (FMOs) along different axes of these cruciforms makes them promising as sensing platforms, since analyte binding to the cruciform should mandate a change in the HOMO–LUMO gap and the resultant optical properties. This prediction was verified using UV/vis absorption and emission spectroscopy: cruciforms’ protonation results in hypsochromic and bathochromic shifts consistent with the preferential stabilization of HOMO and LUMO, respectively. In donor–acceptor-substituted systems, a two-step optical response to protonation was observed, wherein an initial bathochromic shift is followed by a hypsochromic one with continued acidification. X-ray diffraction studies of three selected cruciforms revealed the expected ∼90° angle between the cruciform’s substituents, and crystal packing patterns dominated by [π···π] stacking and edge-to-face [C–H···π] contacts.
Co-reporter:Karolina Osowska ;Ognjen Š. Miljanić
Journal of the American Chemical Society 2010 Volume 133(Issue 4) pp:724-727
Publication Date(Web):December 20, 2010
DOI:10.1021/ja109754t
Dynamic libraries of [n × n] imine components spontaneously simplify during a slow oxidation reaction to produce only n discrete products. The selectivity of this self-sorting process is a consequence of different oxidation rates for various imines, while the dynamic nature of the library enables self-sorting to proceed with high efficiency.
Co-reporter:Karolina Osowska and Ognjen Š. Miljanić  
Chemical Communications 2010 vol. 46(Issue 24) pp:4276-4278
Publication Date(Web):12 May 2010
DOI:10.1039/C0CC00554A
Extended benzobisoxazole-based cruciforms, efficiently synthesized using acyl condensations and Sonogashira couplings, form highly ordered two-dimensional sheets in the solid state.
Co-reporter:Karolina Osowska and Ognjen Š. Miljanić
Chemical Communications 2010 - vol. 46(Issue 24) pp:NaN4278-4278
Publication Date(Web):2010/05/12
DOI:10.1039/C0CC00554A
Extended benzobisoxazole-based cruciforms, efficiently synthesized using acyl condensations and Sonogashira couplings, form highly ordered two-dimensional sheets in the solid state.
Co-reporter:Teng-Hao Chen, Ilya Popov, Oussama Zenasni, Olafs Daugulis and Ognjen Š. Miljanić
Chemical Communications 2013 - vol. 49(Issue 61) pp:NaN6848-6848
Publication Date(Web):2013/06/07
DOI:10.1039/C3CC41564C
Three perfluorinated Cu-based metal–organic frameworks (MOFs) were prepared starting from extensively fluorinated biphenyl-based ligands accessed via C–H functionalization. These new materials are highly hydrophobic: with water contact angles of up to 151 ± 1°, they are among the most water-repellent MOFs ever reported.
Co-reporter:Chia-Wei Hsu and Ognjen Š. Miljanić
Chemical Communications 2016 - vol. 52(Issue 83) pp:NaN12359-12359
Publication Date(Web):2016/09/26
DOI:10.1039/C6CC06772G
Kinetically controlled self-sorting processes in complex synthetic mixtures represent an important model for behaviours of biological networks, which operate far from equilibrium and without interference among simultaneous metabolic pathways. However, most of the previously reported kinetic self-sorting protocols dealt with small dynamic libraries and a single external stimulus. Here, we report the iterative simplification of a large imine dynamic combinatorial library (DCL) constructed from 10 aldehydes and 10 anilines, under the sequential influence of an oxidant, an adsorbent, and an increase in temperature. Six components of this initial DCL are mechanically isolated and amplified at least three-fold relative to their equilibrium distributions at the outset of the sorting process.
Co-reporter:Teng-Hao Chen, Watchareeya Kaveevivitchai, Nghia Bui and Ognjen Š. Miljanić
Chemical Communications 2012 - vol. 48(Issue 23) pp:NaN2857-2857
Publication Date(Web):2012/01/18
DOI:10.1039/C2CC17744G
Mild solvothermal dehydration of 1,1′-ferrocenediboronic acid produces a triply ferrocene-bridged boroxine cyclophane. Its crystal structure reveals a rigid trigonal prism that presents a minimal boroxine-based covalent organic polyhedron (COP).
Co-reporter:Rio Carlo Lirag, Ha T. M. Le and Ognjen Š. Miljanić
Chemical Communications 2013 - vol. 49(Issue 39) pp:NaN4306-4306
Publication Date(Web):2012/10/18
DOI:10.1039/C2CC37120K
Nine L-shaped benzimidazole fluorophores have been synthesized, computationally evaluated and spectroscopically characterized. These “half-cruciform” fluorophores respond to bases, acids and anions through changes in fluorescence that vary from moderate to dramatic.
Co-reporter:Jaebum Lim, Dolly Nam and Ognjen Š. Miljanić
Chemical Science (2010-Present) 2012 - vol. 3(Issue 2) pp:NaN563-563
Publication Date(Web):2011/11/17
DOI:10.1039/C1SC00610J
The fluorescence of a single donor–acceptor benzobisoxazole-based cruciform, dissolved in five different solvents, dramatically changes upon exposure to Brønsted and Lewis acids. The changes in emission colors strongly depend on the analyte's structure, and this cruciform can discern among structurally closely related carboxylic (twelve examples) and organoboronic acids (nine examples). In combination with two commercially available phenylboronic acids, this cruciform sensor also distinguishes among substituted phenols (twelve examples).
Co-reporter:Jaebum Lim and Ognjen Š. Miljanić
Chemical Communications 2012 - vol. 48(Issue 83) pp:NaN10303-10303
Publication Date(Web):2012/09/03
DOI:10.1039/C2CC35626K
A benzobisoxazole-based cruciform fluorophore forms fluorescent complexes with simple boronic acids. Through the changes of their fluorescence emission colours, these complexes can sense and qualitatively distinguish among structurally similar organic nitrogen compounds (amines and ureas) and small organic and inorganic anions. Preliminary results suggest that the intensity of this hybrid sensor's fluorescent response to chloride anions can be quantitatively correlated to chloride concentration.
Co-reporter:Teng-Hao Chen, Watchareeya Kaveevivitchai, Allan J. Jacobson and Ognjen Š. Miljanić
Chemical Communications 2015 - vol. 51(Issue 74) pp:NaN14098-14098
Publication Date(Web):2015/08/04
DOI:10.1039/C5CC04885K
Commonly used inhalation anesthetics—enflurane, isoflurane, sevoflurane, halothane, and methoxyflurane—are adsorbed within the pores of a porous fluorinated molecular crystal to the tune of up to 73.4(±0.2)% by weight. Uptake of all studied anesthetics is quite fast, typically reaching saturation in less than three minutes.
Co-reporter:Qing Ji, Rio Carlo Lirag and Ognjen Š. Miljanić
Chemical Society Reviews 2014 - vol. 43(Issue 6) pp:NaN1884-1884
Publication Date(Web):2014/01/21
DOI:10.1039/C3CS60356C
Dynamic combinatorial libraries (DCLs) are collections of structurally related compounds that can interconvert through reversible chemical reaction(s). Such reversibility endows DCLs with adaptability to external stimuli, as rapid interconversion allows quick expression of those DCL components which best respond to the disturbing stimulus. This Tutorial Review focuses on the kinetically controlled phenomena that occur within DCLs. Specifically, it will describe dynamic chiral resolution of DCLs, their self-sorting under the influence of irreversible chemical and physical stimuli, and the autocatalytic behaviours within DCLs which can result in self-replicating systems. A brief discussion of precipitation-induced phenomena will follow and the review will conclude with the presentation of covalent organic frameworks (COFs)—porous materials whose synthesis critically depends on the fine tuning of the crystal growth and error correction rates within large DCLs.
Co-reporter:Merry K. Smith and Ognjen Š. Miljanić
Organic & Biomolecular Chemistry 2015 - vol. 13(Issue 29) pp:NaN7845-7845
Publication Date(Web):2015/06/25
DOI:10.1039/C5OB01101A
Supramolecular chemistry of conjugated and conformationally rigid arylene ethynylene macrocycles (AEMs) has been the subject of increasing recent interest. AEMs are suited to function as supramolecular building blocks and hosts for small molecular guests thanks to their well-defined, non-collapsible central cavities and the potential for long range ordering through intermolecular π-stacking. Their syntheses are highly modular—albeit typically lengthy—allowing access to a great structural variety of AEM candidates for applications as carbon-rich mesogens and ligands in liquid crystals, nanoporous solids, molecular electronics, and chemical sensors. In this perspective, we highlight our recent work on the inclusion complexes and porous materials constructed from AEMs. Through this prism, we reflect on the recent advances and the remaining challenges in the supramolecular chemistry of AEMs.
Co-reporter:Rio Carlo Lirag and Ognjen Š. Miljanić
Chemical Communications 2014 - vol. 50(Issue 66) pp:NaN9404-9404
Publication Date(Web):2014/07/01
DOI:10.1039/C4CC02990A
Four acid-catalysed dehydration reactions can proceed in one pot, simultaneously and without interference, to yield one imine, one acetal (or boronic ester), one ester and one alkene, even though many other cross-products could be conceived. This advanced self-sorting behaviour is attributed to different dehydration rates, brought about by dissimilar electronic properties of starting materials.
Co-reporter:Virginia Martínez-Martínez, Jaebum Lim, Jorge Bañuelos, Iñigo López-Arbeloa and Ognjen Š. Miljanić
Physical Chemistry Chemical Physics 2013 - vol. 15(Issue 41) pp:NaN18029-18029
Publication Date(Web):2013/09/23
DOI:10.1039/C3CP53527D
A photophysical study was carried out on a series of nine X-shaped cross-conjugated compounds based on the benzobisoxazole nucleus. These “molecular cruciforms” were terminally substituted with electron-rich 4-(N,N-dimethylamino)phenyl, electron-neutral phenyl or electron-poor 4-pyridyl groups. Intramolecular charge transfer (ICT) transitions in molecular cruciforms were shown to be activated to a different extent by the combinations of these substituents located in different positions along vertical and/or horizontal axes of the molecules, showing strong emission throughout the visible spectrum. The high fluorescence efficiency and bathochromic shifts associated with the increasing polarity of the solvent make these cruciforms interesting candidates for use as fluorescence polarity indicators operating in a broad solvatochromic range.
Co-reporter:Teng-Hao Chen, Ilya Popov, Yu-Chun Chuang, Yu-Sheng Chen and Ognjen Š. Miljanić
Chemical Communications 2015 - vol. 51(Issue 29) pp:NaN6342-6342
Publication Date(Web):2015/03/04
DOI:10.1039/C5CC01635E
A mesoporous Zn-based metal–organic framework (MOF) was prepared from a shape-persistent phenylene ethynylene macrocycle functionalized with three –COOH groups. The rigid ligand has a ∼9 Å wide central cavity which serves as a predesigned pore. The macrocycles [π⋯π] stack into pairs, with their carboxylate groups connected via three Zn3O14C6H2 clusters. The resulting MOF has a void volume of 86%.
Co-reporter:Rio Carlo Lirag, Karolina Osowska and Ognjen Š. Miljanić
Organic & Biomolecular Chemistry 2012 - vol. 10(Issue 25) pp:NaN4850-4850
Publication Date(Web):2012/05/21
DOI:10.1039/C2OB25736J
Judicious choice of precipitation conditions can lead to self-sorting of equilibrating mixtures of aromatic aldehydes and substituted anilines into a handful of imine products. The selectivity of this process is caused by the solubility differences among possible imines in the EtOH–H2O solvent mixtures used in precipitation.
Benzenamine, 4-(octyloxy)-N-[[4-(octyloxy)phenyl]methylene]-
BENZENAMINE, 4-CHLORO-N-[(2-METHYLPHENYL)METHYLENE]-
N-[(4-nitrophenyl)methylene]-4-(octyloxy)benzenamine
1-(4-BROMOPHENYL)-N-(4-CHLOROPHENYL)METHANIMINE
Benzenamine, 4-bromo-N-[(4-chlorophenyl)methylene]-
Benzenamine, N-[(4-chlorophenyl)methylene]-4-methyl-
4-chloro-N-[(E)-(4-chlorophenyl)methylidene]aniline
Benzenamine, N-[(2-methylphenyl)methylene]-
Benzoic acid, 2,3,5,6-tetrafluoro-, 1,1-dimethylethyl ester