thienothiophene cages

교원검색
The Role of water cages and hydrophobic interaction in phase transition, 한국고분자학회 연구논문초록집, 0, 0, 58- (2001) A study of adhesion behavior of triblock copolymer/rosin blend system using contact-based-mechanics, 한국고분자학회 연구논문초록집, 0, 0, 244- (2001)

Publications
However, a diketopyrrolopyrrole-thienothiophene copolymer shows remarkably high optical absorption at relatively low photon energies. By investigating its backbone structure and conformation with measurements and quantum chemical calculations, we find that the high optical absorption can be explained by the high persistence length of the polymer.

Publications
However, a diketopyrrolopyrrole-thienothiophene copolymer shows remarkably high optical absorption at relatively low photon energies. By investigating its backbone structure and conformation with measurements and quantum chemical calculations, we find that the high optical absorption can be explained by the high persistence length of the polymer.

2019 publications citing ADF
2019 publications citing ADF First author: Wen, M, OBCN isomerization and noble gas insertion compounds of identical valence electron number species: stability and bonding, PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 21, 26311, (2019) Abstract: A series of new noble gas (Ng) insertion compounds of the general type XNgX, XNgY and XNgY(+) has been theoretically studied using ab initio and DFT

Room
Cu-BBTC features a three-dimensional fof network with two types of cages, a small cage is about 14 in diameter and a large shows an ellipsoidal pore with about 14.222.6 in axes. The activated sample of Cu-BBTC, with Langmuir surface area of 1569 m{sup 2} g{sup −1}, exhibits selective gas adsorption behavior with respect to C{sub 2}H{sub 2}/CH{sub 4} and CO{sub 2}/CH{sub 4} at room

Nanoniele
thienothiophene ( TT) (1) Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages ( Chem. Sci. 2021, Advance Article, −; 10.1039/D1SC00440A ) TT (2) Indacenodithiophene (IDT) and indacenodithienothiophene (IDTT)-based acceptors for non-fullerene organic solar cells ( Synth.

transistors with enhanced electrical stability Densely cross
Electronic Supplementary Information Densely cross-linked polysiloxane dielectric for organic thin-film transistors with enhanced electrical stability Joo-Young Kim,a,b‡ Eun Kyung Lee,a‡ Jiyoung Jung,a Don-Wook Lee,a Youngjun Yun,a Jong Won Chung,a Jeong-Il Park,a and Jang-Joo Kim*b

Selective Adsorption and Separation of Xylene Isomers and
The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acsami.8b11657.Synthesis scheme and 1 H NMR spectra of the modified triptycene monomers, XRD pattern, TGA curve, UV–vis spectra for Bz and , adsorption and desorption cycles for Bz and mX of POP-1, electrostatic potential maps, theoretical results (host–guest energy and optimized

2014 publications citing ADF
The hydrogen bond is shorter in confined cages than that in free dimer. The interaction energy between two HF units is maximum in Cgo whereas the bond is the shortest in C-70. It appears that in confined situation a shorter bond does not necessarily mean a stronger bond.

Soft Porous Crystal Based upon Organic Cages That
Soft porous crystals (SPCs) that exhibit stimuli-responsive dynamic sorption behavior are attracting interest for gas storage/separation applications. However, the design and synthesis of SPCs is challenging. Herein, we report a new type of SPC based on a [2 + 3] imide-based organic cage (NKPOC-1) and find that it exhibits guest-induced breathing behavior. Various gases were found to induce

Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages
In this work, we report an environmentally friendly and energy saving approach to separate Cy over Bz using thienothiophene cages (ThT-cages) with adaptive porosity. Interestingly, cyclohexane was readily captured selectively from an equimolar benzene/cyclohexane mixture with a purity of 94%.

Progress in Chemistry
Again, the steric effect between the two N-linked alkyl chains and the decorated chains on the fused thienothiophene-β-positions helped to increase the solubility and tune crystallinity. After the report of the smart Y6, intense investigations have been made on structure cutting of the molecule and tens of new structures have been reported.

Nanoniele
thienothiophene ( TT) (1) Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages ( Chem. Sci. 2021, Advance Article, −; 10.1039/D1SC00440A ) TT (2) Indacenodithiophene (IDT) and indacenodithienothiophene (IDTT)-based acceptors for non-fullerene organic solar cells ( Synth.

Picric acid sensing and $$hbox {CO}_{2}$$ CO 2 capture by
1. (a) Nagarkar S S, Joarder B, Chaudhari A K, Mukherjee S and Ghosh S K 2013 Highly selective detection of nitro explosives by a luminescent metal–organic framework Angew.Chem. Int. Edit. 52 2881; (b) Madhu S, Bandela A and Ravikanth M 2014 Bodipy based fluorescent chemodosimeter for explosive picric acid in aqueous media and rapid detection in the solid state RSC Adv. 4 7120; (c) Dinda D

Intrinsically Porous Molecular Materials (IPMs) for Natural
ConspectusSeparating and purifying chemicals without heat would go a long way toward reducing the overall energy consumption and the harmful environmental footprint of the process. Molecular separation processes are critical for the production of raw materials, commodity chemicals, and specialty fuels. Over 50% of the energy used in the production of these materials is spent on separation and

2017 publications citing ADF
Optical calculations showed that thienothiophene extension cannot affect the Stokes shifts of thienothiophene derivatives. Importantly, it is found that the hole mobility of thienothiophene molecules is co-determined by the molecular size and odd or even number of thiophthene units, and all investigated thienothiophene molecules show higher hole mobility than Sprio-OMeTAD due to the face-to

Separation of Benzene and Cyclohexane by Nonporous
The separation of benzene and cyclohexane is one of the most challenging tasks in the petrochemical field. However, conventional separation methods suffer from cumbersome operation, huge energy expenditure, or use of entrainers. Herein, we develop an environmentally friendly and energy saving adsorptive separation strategy using nonporous adaptive crystals of a hybrid[3]arene (1). Adaptive 1

Tuning photoactive metal–organic frameworks for
The Lewis-basic sulfur sites of the thienothiophene linker were identified as potential coordination sites for the selective chelation of metal ions. IFMC-28 showed selective adsorption of Cu II ions over other metal ions, such as Pb II, Ni II, Co II, Mn II, Mg II and Cd II ions ( Fig. 8 b)).

Advances in the Synthesis of Organoborane Polymers
Supramolecular Pt(II) and Ru(II) Trigonal Prismatic Cages Constructed with a Tris(pyridyl)borane Donor Ji Yeon Ryu Ji Min Lee Nguyen Van Nghia Kang Mun Lee Sunwoo Lee Min Hyung Lee Peter J. Stang Junseong Lee Inorganic Chemistry 2018 57 Abstract

2019 publications citing ADF
2019 publications citing ADF First author: Wen, M, OBCN isomerization and noble gas insertion compounds of identical valence electron number species: stability and bonding, PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 21, 26311, (2019) Abstract: A series of new noble gas (Ng) insertion compounds of the general type XNgX, XNgY and XNgY(+) has been theoretically studied using ab initio and DFT

Selective adsorptive separation of cyclohexane over
Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages† Yanjun Ding a, Lukman O. Alimi a, Basem Moosa a, Carine Maaliki b, Johan Jacquemin b, Feihe Huang c and Niveen M. Khashab * a a Smart Hybrid Materials (SHMs) Laboratory, Advanced Membranes and Porous Materials Center, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900,

Advances in the Synthesis of Organoborane Polymers
Supramolecular Pt(II) and Ru(II) Trigonal Prismatic Cages Constructed with a Tris(pyridyl)borane Donor Ji Yeon Ryu Ji Min Lee Nguyen Van Nghia Kang Mun Lee Sunwoo Lee Min Hyung Lee Peter J. Stang Junseong Lee Inorganic Chemistry 2018 57 Abstract

Publications
However, a diketopyrrolopyrrole-thienothiophene copolymer shows remarkably high optical absorption at relatively low photon energies. By investigating its backbone structure and conformation with measurements and quantum chemical calculations, we find that the high optical absorption can be explained by the high persistence length of the polymer.

Publications
However, a diketopyrrolopyrrole-thienothiophene copolymer shows remarkably high optical absorption at relatively low photon energies. By investigating its backbone structure and conformation with measurements and quantum chemical calculations, we find that the high optical absorption can be explained by the high persistence length of the polymer.

Soft Porous Crystal Based upon Organic Cages That Exhibit
Soft porous crystals (SPCs) that exhibit stimuli-responsive dynamic sorption behavior are attracting interest for gas storage/separation applications. However, the design and synthesis of SPCs is challenging. Herein, we report a new type of SPC based on a [2 + 3] imide-based organic cage (NKPOC-1) and find that it exhibits guest-induced breathing behavior. Various gases were found to induce

Selective adsorptive separation of cyclohexane over benzene using
Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages† Yanjun Ding,a Lukman O. Alimi,a Basem Moosa,a Carine Maaliki,b Johan Jacquemin, b Feihe Huang c and Niveen M. Khashab *a The selective separation of benzene (Bz

Nanoniele
thienothiophene ( TT) (1) Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages ( Chem. Sci. 2021, Advance Article, −; 10.1039/D1SC00440A ) TT (2) Indacenodithiophene (IDT) and indacenodithienothiophene (IDTT)-based acceptors for non-fullerene organic solar cells ( Synth.

Porous Shape
ConspectusThe interest in shape-persistent organic cages is nearly as old as the interest in supramolecular chemistry. In the beginning, organic cages have often been synthesized in a stepwise manner, which is not only laborious but very often also accompanied by low overall yields. In 1988, MacDowell published the one pot high-yielding synthesis of [2 + 3] imine cages based on TREN and