wtorek, 27 kwietnia 2010

A One-Step Synthesis of 2,4-Unsubstituted Quinoline-3-carboxylic Acid Esters from o-Nitrobenzaldehydes


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A One-Step Synthesis of 2,4-Unsubstituted Quinoline-3-carboxylic Acid Esters from o-Nitrobenzaldehydes

The Journal of Organic Chemistry, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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Self-Assembly of Flexible One-Dimensional Coordination Polymers on Metal Surfaces


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Self-Assembly of Flexible One-Dimensional Coordination Polymers on Metal Surfaces

Journal of the American Chemical Society, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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n → π* Interaction and n)(π Pauli Repulsion Are Antagonistic for Protein Stability


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n → π* Interaction and n)(π Pauli Repulsion Are Antagonistic for Protein Stability

Journal of the American Chemical Society, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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piątek, 23 kwietnia 2010

Periodic bond breaking and making in the electronic ground state on a sub-picosecond timescale: OH bending spectroscopy of malonaldehyde in the frequency domain at low temperature


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Periodic bond breaking and making in the electronic ground state on a sub-picosecond timescale: OH bending spectroscopy of malonaldehyde in the frequency domain at low temperature


Nils O. B. Luttschwager, Tobias N. Wassermann, Stephane Coussan, Martin A. Suhm

(Paper from Phys. Chem. Chem. Phys.)

Nils O. B. Luttschwager, Phys. Chem. Chem. Phys., 2010, DOI: 10.1039/c002345k

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Complementary double helix formation through template synthesis


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Complementary double helix formation through template synthesis


Hidekazu Yamada, Yoshio Furusho, Hiroshi Ito, Eiji Yashima

(Communication from Chem. Commun.)

Hidekazu Yamada, Chem. Commun., 2010, DOI: 10.1039/c002170a

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Efficient Pd-Catalyzed Coupling of Tautomerizable Heterocycles with Terminal Alkynes via C−OH Bond Activation Using PyBrOP


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Efficient Pd-Catalyzed Coupling of Tautomerizable Heterocycles with Terminal Alkynes via C−OH Bond Activation Using PyBrOP

Organic Letters, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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Hydrogen Bonding in Organic Synthesis


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Hydrogen Bonding in Organic Synthesis

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czwartek, 22 kwietnia 2010

środa, 21 kwietnia 2010

Comparison of cationic, anionic and neutral hydrogen bonded dimers


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Comparison of cationic, anionic and neutral hydrogen bonded dimers


Han Myoung Lee, Anupriya Kumar, Maciej Kolaski, Dong Young Kim, Eun Cheol Lee, Seung Kyu Min, Mina Park, Young Cheol Choi, Kwang S. Kim

(Paper from Phys. Chem. Chem. Phys.)

Han Myoung Lee, Phys. Chem. Chem. Phys., 2010, DOI: 10.1039/b925551f

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Host-guest assembly of squaraine dye in cucurbit[8]uril: its implication in fluorescent probe for mercury ions


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Host-guest assembly of squaraine dye in cucurbit[8]uril: its implication in fluorescent probe for mercury ions


Yongqian Xu, Matthew J. Panzner, Xiaopeng Li, Wiley J. Youngs, Yi Pang

(Communication from Chem. Commun.)

Yongqian Xu, Chem. Commun., 2010, DOI: 10.1039/c002219p

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Directional hydrogen bonding controlled 2D self-organization of phenyleneethynylenes: from linear assembly to rectangular network


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Directional hydrogen bonding controlled 2D self-organization of phenyleneethynylenes: from linear assembly to rectangular network


A. R. Ramesh, K. George Thomas

(Communication from Chem. Commun.)

A. R. Ramesh, Chem. Commun., 2010, DOI: 10.1039/b927281j

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Highly Selective Visual Detection of Cu(II) Utilizing Intramolecular Hydrogen Bond-Stabilized Merocyanine in Aqueous Buffer Solution


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Highly Selective Visual Detection of Cu(II) Utilizing Intramolecular Hydrogen Bond-Stabilized Merocyanine in Aqueous Buffer Solution

Organic Letters, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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piątek, 16 kwietnia 2010

Supramolecular Polymers

 
 

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Tom F.A. de Greef, E. W. Meijer - Volume 63(4)

In the past few decades, supramolecular polymers have emerged as novel materials with a wide variety of different functions. In this essay we reflect on the history of supramolecular polymers, their function in various applications and the challenges to be met in the near future.



 
 

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Binary complexes of tertiary amines with phenylacetylene. Dispersion wins ov...

 
 

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przez RSC - Phys. Chem. Chem. Phys. latest articles autor: Kwang S. Kim dnia 10-04-13

Surajit Maity, G. Naresh Patwari, S. Karthikeyan, Kwang S. Kim
(Paper from Phys. Chem. Chem. Phys.)
Surajit Maity, Phys. Chem. Chem. Phys., 2010, DOI: 10.1039/b918013c
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Inversion of the shuttlecock shaped metal phthalocyanines MPc (M = Ge, Sn, P...

 
 

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przez RSC - Phys. Chem. Chem. Phys. latest articles autor: J. Andreas Larsson dnia 10-04-14

Jakub D. Baran, J. Andreas Larsson
(Paper from Phys. Chem. Chem. Phys.)
Jakub D. Baran, Phys. Chem. Chem. Phys., 2010, DOI: 10.1039/b924421b
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Long wavelength red fluorescent dyes from 3,5-diiodo-BODIPYs

 
 

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przez RSC - Org. Biomol. Chem. latest articles autor: M. Graca H. Vicente dnia 10-04-14

Lijuan Jiao, Changjiang Yu, Timsy Uppal, Mingming Liu, Yan Li, Yunyou Zhou, Erhong Hao, Xiaoke Hu, M. Graca H. Vicente
(Communication from Org. Biomol. Chem.)
Lijuan Jiao, Org. Biomol. Chem., 2010, DOI: 10.1039/c001068e
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Specific Cu2+-induced J-aggregation and Hg2+-induced fluorescence enhancemen...

 
 

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przez RSC - Chem. Commun. latest articles autor: Nagao Kobayashi dnia 10-04-15

Hua Lu, Zhaoli Xue, John Mack, Zhen Shen, Xiaozeng You, Nagao Kobayashi
(Communication from Chem. Commun.)
Hua Lu, Chem. Commun., 2010, DOI: 10.1039/b926300d
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Two-dimensional polyphenylene: experimentally available porous graphene as a...

 
 

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przez RSC - Chem. Commun. latest articles autor: Zhongfang Chen dnia 10-04-15

Yafei Li, Zhen Zhou, Panwen Shen, Zhongfang Chen
(Communication from Chem. Commun.)
Yafei Li, Chem. Commun., 2010, DOI: 10.1039/b926313f
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czwartek, 15 kwietnia 2010

Synthesis and Characterization of BODIPY-α-Tocopherol: A Fluorescent Form of Vitamin E


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Synthesis and Characterization of BODIPY-α-Tocopherol: A Fluorescent Form of Vitamin E

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A Xenon-Based Molecular Sensor Assembled on an MS2 Viral Capsid Scaffold


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A Xenon-Based Molecular Sensor Assembled on an MS2 Viral Capsid Scaffold

Journal of the American Chemical Society, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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poniedziałek, 12 kwietnia 2010

An Effective Method for Studying Intermolecular Interactions in Binary Liquids with Hydrogen Bonds; FTIR Spectra and Ab Initio Calculations in the N-Methylformamide−Methanol System


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An Effective Method for Studying Intermolecular Interactions in Binary Liquids with Hydrogen Bonds; FTIR Spectra and Ab Initio Calculations in the N-Methylformamide−Methanol System

The Journal of Physical Chemistry B, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).


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RAFT polymerization of luminescent boron quinolate monomers


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RAFT polymerization of luminescent boron quinolate monomers


Fei Cheng, Frieder Jakle

(Communication from Chem. Commun.)

Fei Cheng, Chem. Commun., 2010, DOI: 10.1039/b920667a

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niedziela, 11 kwietnia 2010

Resorcin[4]arene cavitand with 1,3,2-benzodiazaborolyl walls as a fluorescen...

 
 

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przez RSC - Chem. Commun. latest articles autor: Takashi Fujihara dnia 10-04-09

Yuji Kubo, Kazusa Tsuruzoe, Sachiko Okuyama, Ryuhei Nishiyabu, Takashi Fujihara
(Communication from Chem. Commun.)
Yuji Kubo, Chem. Commun., 2010, DOI: 10.1039/c0cc00259c
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sobota, 10 kwietnia 2010

Cascade Cyclization To Produce a Series of Fused, Aromatic Molecules

 
 

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przez Organic Letters: Latest Articles (ACS Publications) autor: William J. Behof et al dnia 10-04-08

Organic Letters, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).

 
 

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Solute Descriptors for Phenoxide Anions and Their Use To Establish Correlati...

 
 

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przez The Journal of Organic Chemistry: Latest Articles (ACS Publications) autor: Michael H. Abraham et al dnia 10-04-09

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niedziela, 4 kwietnia 2010

meso-Trifluoromethyl-substituted Subporphyrin from Ring-splitting Reaction of meso-Trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1)



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Luminescent Organoboron Conjugated Polymers


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Luminescent Organoboron Conjugated Polymers


The incorporation of luminescent organoboron dyes into π-conjugated polymer backbones is attractive for potential applications as electroluminescent devices, organic field-effect transistors, and photovoltaics. We have developed various boron π-conjugated polymers by introduction of stable tetracoordinated organoboron dyes into π-conjugated polymer backbones to afford more stable and higher luminescent conjugated polymers than three-coordinated organoboron polymers. Recent advances in the field of organoboron polymers are reviewed here.


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