Ambient pressure XPS on the cheap

X-ray photoelectron spectroscopy (XPS) is capable of characterising the surface composition, oxidation state and electron state of materials. Unfortunately, it uses electrons and so common XPS machines must work at vacuum pressures. But how could you use XPS under ambient pressure?

One option would be to use public synchrotron facilities but access is through proposal review and available time is restricted so it is not feasible for day-to-day studies. Another option would be to follow the lead of Franklin Tao and build an inexpensive, ambient pressure XPS machine in-house.

Such a machine is ideal for catalytic studies. Previously scientists investigated catalysts with conventional vacuum XPS before and after experiments. Tao’s machine enables him to investigate catalyst surface changes during reaction conditions, something that required synchrotron facilities until now. The machine’s novel reaction cell allows XPS measurements to be carried out at up to 25-50 Torr using an inexpensive bench top X-ray source.

external view of the reaction cell
external view of the reaction cell

In addition to the ambient pressure XPS functionality, an on-line mass spectrometer allows correlation between catalytic performance and surface chemistry. Tao has demonstrated this novel machine by investigating the oxidation and reduction of ceria under real reaction conditions.

With day-to-day ambient pressure XPS now within reach of every research group, catalytic studies under reaction conditions have received a significant boost.

To find out more, download the ChemComm article today.

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Stopping bugs in their tracks

To prevent the spread of bugs, scientists in Switzerland have starved microbes of phosphate by using lanthanum oxide nanoparticles. The nanoparticles compete against the microbes for available phosphate and so the microbes can’t grow. The team says that the strategy is of particular technical interest as it can bypass toxic material release and provides an antimicrobial solution with small environmental footprint.

Phosphate starvation as an antimicrobial strategy

Link to journal article
Phosphate starvation as an antimicrobial strategy: the controllable toxicity of lanthanum oxide nanoparticles
L C Gerber et al
Chem. Commun., 2012, DOI: 10.1039/c2cc30903c

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Top ten most accessed articles in February

This month sees the following articles in ChemComm that are in the top ten most accessed:-

Transition metal catalysis and nucleophilic fluorination
Charlotte Hollingworth and Véronique Gouverneur
Chem. Commun., 2012, 48, 2929-2942, DOI: 10.1039/C2CC16158C

Use of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalysts
Kiyofumi Inamoto, Chisa Hasegawa, Kou Hiroya, Yoshinori Kondo, Takao Osako, Yasuhiro Uozumi and Takayuki Doi
Chem. Commun., 2012, 48, 2912-2914, DOI: 10.1039/C2CC17401D

Pd-catalysed synthesis of isoquinolinones and analogues via C-H and N-H bonds double activation
Hongban Zhong, Dan Yang, Songqing Wang and Jianhui Huang
Chem. Commun., 2012, 48, 3236-3238, DOI: 10.1039/C2CC17859A

Photoisomerization locking of azobenzene by formation of a self-assembled macrocycle
Masaki Yamamura, Yuki Okazaki and Tatsuya Nabeshima
Chem. Commun., 2012, Advance Article, DOI: 10.1039/C2CC18014F

Highly selective red- and green-emitting two-photon fluorescent probes for cysteine detection and their bio-imaging in living cells
Zhiguang Yang, Ning Zhao, Yuming Sun, Fang Miao, Yong Liu, Xin Liu, Yuanhong Zhang, Wentao Ai, Guofen Song, Xiaoyuan Shen, Xiaoqiang Yu, Jingzhi Sun and Wai-Yeung Wong
Chem. Commun., 2012, 48, 3442-3444, DOI: 10.1039/C2CC00093H

A reversible near-infrared fluorescence probe for reactive oxygen species based on Te-rhodamine
Yuichiro Koide, Mitsuyasu Kawaguchi, Yasuteru Urano, Kenjiro Hanaoka, Toru Komatsu, Masahiro Abo, Takuya Terai and Tetsuo Nagano
Chem. Commun., 2012, 48, 3091-3093, DOI: 10.1039/C2CC18011A

A supramolecular hydrogel containing boronic acid-appended receptor for fluorocolorimetric sensing of polyols with a paper platform
Masato Ikeda, Keisuke Fukuda, Tatsuya Tanida, Tatsuyuki Yoshii and Itaru Hamachi
Chem. Commun., 2012, 48, 2716-2718, DOI: 10.1039/C2CC17503G

N-Heterocyclic carbene chemistry of iron: fundamentals and applications
Michael J. Ingleson and Richard A. Layfield
Chem. Commun., 2012, 48, 3579-3589, DOI: 10.1039/C2CC18021A

Reversible formal insertion of CO2 into a remote C-H bond of a ligand in a Ru(ii) complex at room temperature
Vincent T. Annibale and Datong Song
Chem. Commun., 2012, Advance Article, DOI: 10.1039/C2CC17933D

A turn-on two-photon fluorescent probe for ATP and ADP
Alla Sreenivasa Rao, Dokyoung Kim, Hyoseok Nam, Hunho Jo, Ki Hean Kim, Changill Ban and Kyo Han Ahn
Chem. Commun., 2012, 48, 3206-3208, DOI: 10.1039/C2CC17629G

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to ChemComm? Then why not submit to us today or alternatively contact us with your suggestions.

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Cheap and non-toxic porphyrins for detecting cells deep within the body

Near-infrared fluorescent imaging can be used for rapid and sensitive detection of cells deep within the body. However, common NIR dyes and quantum dots are expensive and/or toxic.

Porphyrins are economical fluorescent dyes, but their emission and excitation wavelengths are shorter than the NIR region and they can be toxic and poorly water-soluble. Scientists in Japan have made silica–porphyrin hybrid nanotubes that have no acute toxicity and higher water solubility compared to porphyrin. They used them to label macrophages, injected them into mice and tracked their distribution by fluorescence imaging with good results.

c2cc17444h

Link to journal article
Silica/Porphyrin Hybrid Nanotubes for In Vivo Cell Tracking by Near-Infrared Fluorescence Imaging
K Hayashi, M Nakamura and K Ishimura
Chem. Commun., 2012, DOI: 10.1039/c2cc17444h

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Micro power for micro devices

An easy way to make high-performance micro-supercapacitors based on nanocrystal building blocks has been developed by scientists in the US and China. Micro-power sources have become a key component for micro-electronics but they are expensive and difficult to make. To demonstrate their concept, the team made nanoporous thin-film pseudocapacitor electrodes that showed ultrafast lithium storage kinetics, high capacitance and excellent cycling stability, giving them great promise for high energy and high power micro-device applications.

c2cc30406f

Link to journal article
Ready Fabrication of Thin-Film Electrodes from Building Nanocrystals for Micro-Supercapacitors
Z Chen et al
Chem. Commun., 2012, DOI: 10.1039/c2cc30406f

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Hydrogen storage material reaches 12wt% release of pure hydrogen at moderate temperature

Ammine aluminium borohydrides are promising materials for hydrogen storage but they have low hydrogen capacities and sluggish kinetics under moderate temperatures.

 

Now, by changing the coordination number of ammonia and adopting mixed cations, scientists in China have found an ammine aluminium borohydride that releases over 12wt% of pure hydrogen at 120oC. This is well above the minimum abundance of hydrogen required for on-board applications, they say.

c2cc30751k

 

Link to journal article
Ammine aluminum borohydrides: an appealing system releasing over 12 wt.% pure H2 under moderate temperature

Y Guo et al
Chem Commun., 2012, DOI: 10.1039/c2cc30751k

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Sustainable Inorganic Chemistry Symposium at Spring ACS Meeting

Sustainable Inorganic Chemistry Symposium

We are delighted to announce the forthcoming Symposium on Sustainable Inorganic Chemistry sponsored by ChemComm and the ACS Division of Inorganic Chemistry, which will be held at the ACS Spring 2012 National Meeting & Exposition.

Date: 25-27 March 2012
Location: San Diego Convention Center – Room 9, San Diego, USA

With 22 invited talks across three days by both world-leading authorities and incredibly talented emerging researchers, the symposium will cover CO2 capture and recycle; energy storage; photovoltaics; water purification; unconventional resources; and energy efficiency, all of which are underpinned by inorganic chemistry.

View the schedule >

ChemComm Editor Robert Eagling is co-organiser of the symposium – let him know if you plan to attend.

Twitter Bird@ChemCommun               Follow the symposium at #CCsymp

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ChemComm–RSC Prizes and Awards Symposium in Oxford

Free-to-attend meeting focusing on inorganic and supramolecular chemistry

We are delighted to announce the forthcoming ChemComm–RSC Prizes & Awards Symposium jointly organised with the RSC Dalton Division.

Date: Wednesday 23rd May 2012
Location: University of Oxford, UK
Time: 11am – 6.45 pm

The purpose of this event is to bring together scientists in a stimulating and friendly environment to recognise the achievements of individuals in advancing the chemical sciences and also to foster collaborations. The symposium will appeal to academic and industrial scientists with an interest in inorganic and supramolecular chemistry. Attendance at the symposium is FREE OF CHARGE and student participation is strongly encouraged.

The following distinguished scientists have agreed to speak:

To register for the symposium, please complete the online registration form.

For further details, please contact Richard Walker.

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ChemComm Emerging Investigator Lectureship 2012: The winner is….

Recognising and rewarding the very best emerging talent within the chemical sciences

Hiromitsu MaedaOn behalf of the ChemComm Editorial Board, I am delighted to announce that Professor Hiromitsu Maeda (Ritsumeikan University, Japan) has won the ChemComm Emerging Investigator Lectureship 2012.

This annual award recognises an emerging scientist in the early stages of their independent academic career. The Editorial Board commended Professor Maeda’s contributions to the fields of organic chemistry, supramolecular chemistry and materials science.

‘Maeda is doing extremely exciting and innovative work in soft materials and particularly switchable gels chemistry,’ says ChemComm Associate Editor Jonathan Steed. ‘As one of the first people to recognise that gel rheology can be switched by simple host guest interactions, he has recently produced a startling and exquisite range of highly engineered compounds showing fascinating properties as smart materials.’

Further details of Professor Maeda’s lectureship, including lecture locations, will be announced soon.

To find out more about Professor Maeda’s work, read some of his latest articles:
Charge-based and charge-free molecular assemblies comprising π-extended derivatives of anion-responsive acyclic oligopyrroles
Yuya Bando, Shohei Sakamoto, Ippei Yamada, Yohei Haketa and Hiromitsu Maeda
Chem. Commun., 2012, 48, 2301-2303

Solid-state supramolecular assemblies consisting of planar charged species
Yohei Haketa, Mayumi Takayama and Hiromitsu Maeda
Org. Biomol. Chem., 2012, DOI: 10.1039/C2OB07059F

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Chiral self-recognition by simple macrocycles

A recent communication from Isao Azumaya, Aya Tanatani and colleagues describes their work on some macrocycles based on cyclic triamide 1. The bowl-like structure of these macrocycles is reminiscent of well-known supramolecular building blocks such as calixarenes, and the authors hope that they might be similarly applied to constructing supramolecular architectures. These macrocycles have three possible inter-convertible conformations, of which the most stable syn- forms are enantiomeric.

Structure and conformations of cyclic triamide 1 

The group found that a number of triamide-substituted macrocycles such as 2 dimerise into capsule-like structures in the solid state through interactions between the amide groups. Remarkably, 2 formed chiral crystals, as the macrocycles dimerised in the syn-form and only with their own enantiomer. This is the first report of the separation of cyclic triamides without using an additional chiral species, and shows that this particular macrocycle is able to recognise its own enantiomer (in the figure below single enantiomers are shown in the same colour).

cyclic triamide

In solution, a tricarboxylate-substituted macrocycle was shown to interact with a chiral amine guest. This caused induction of chirality in a host in which, in equilibrium in solution, no particular enantiomer is usually favoured.

These simple macrocycles are easy to synthesise and functionalise and have fascinating dynamic behaviour in solution and in the solid state. They are an exciting prospect for application as molecular building blocks with the added potential for host-guest chemistry.

Find out more download the communication for free for limited period.

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