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Cationic terminal borylene complexes: Interconversion of amino and alkoxy borylenes by an unprecedented Meerwein-Ponndorf hydride transfer.

Angewandte Chemie (International ed. in English)

Kays DL, Day JK, Aldridge S, Harrington RW, Clegg W.
PMID: 16634104
Angew Chem Int Ed Engl. 2006 May 19;45(21):3513-6. doi: 10.1002/anie.200600714.

No abstract available.

Cite
Kays DL, Day JK, Aldridge S, et al. Cationic terminal borylene complexes: Interconversion of amino and alkoxy borylenes by an unprecedented Meerwein-Ponndorf hydride transfer. Angew Chem Int Ed Engl. 2006;45(21):3513-6doi: 10.1002/anie.200600714.
Kays, D. L., Day, J. K., Aldridge, S., Harrington, R. W., & Clegg, W. (2006). Cationic terminal borylene complexes: Interconversion of amino and alkoxy borylenes by an unprecedented Meerwein-Ponndorf hydride transfer. Angewandte Chemie (International ed. in English), 45(21), 3513-6. https://doi.org/10.1002/anie.200600714
Kays, Deborah L, et al. "Cationic terminal borylene complexes: Interconversion of amino and alkoxy borylenes by an unprecedented Meerwein-Ponndorf hydride transfer." Angewandte Chemie (International ed. in English) vol. 45,21 (2006): 3513-6. doi: https://doi.org/10.1002/anie.200600714
Kays DL, Day JK, Aldridge S, Harrington RW, Clegg W. Cationic terminal borylene complexes: Interconversion of amino and alkoxy borylenes by an unprecedented Meerwein-Ponndorf hydride transfer. Angew Chem Int Ed Engl. 2006 May 19;45(21):3513-6. doi: 10.1002/anie.200600714. PMID: 16634104.
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Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid-base pairs.

Chemical communications (Cambridge, England)

Morgan IR, Di Paolo A, Vidovic D, Fallis IA, Aldridge S.
PMID: 20024204
Chem Commun (Camb). 2009 Dec 21;(47):7288-90. doi: 10.1039/b917304h. Epub 2009 Nov 04.

A facile synthetic approach is reported for the synthesis of dissymmetric 1,2-ferrocenediyl Lewis acids and mixed acid-base pairs including the first example of a 1-phosphino-2-borylferrocene; the use of non-racemic electrophiles allows for the isolation of single diastereomer products.

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Morgan IR, Di Paolo A, Vidovic D, et al. Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid-base pairs. Chem Commun (Camb). 2009;(47):7288-90doi: 10.1039/b917304h.
Morgan, I. R., Di Paolo, A., Vidovic, D., Fallis, I. A., & Aldridge, S. (2009). Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid-base pairs. Chemical communications (Cambridge, England), (47), 7288-90. https://doi.org/10.1039/b917304h
Morgan, Ian R, et al. "Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid-base pairs." Chemical communications (Cambridge, England) vol. ,47 (2009): 7288-90. doi: https://doi.org/10.1039/b917304h
Morgan IR, Di Paolo A, Vidovic D, Fallis IA, Aldridge S. Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid-base pairs. Chem Commun (Camb). 2009 Dec 21;(47):7288-90. doi: 10.1039/b917304h. Epub 2009 Nov 04. PMID: 20024204.
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Reprint--AACVPR/ACCF/AHA 2010 update: performance measures on cardiac rehabilitation for referral to cardiac rehabilitation/secondary prevention services: a report of the American Association of Cardiovascular and Pulmonary Rehabilitation and the American College of Cardiology Foundation/American Heart Association Task Force on Performance Measures (Writing Committee to Develop Clinical Performance Measures for Cardiac Rehabilitation).

Physical therapy

Thomas RJ, King M, Lui K, Oldridge N, Piña IL, Spertus J, Masoudi FA, DeLong E, Erwin JP, Goff DC, Grady K, Green LA, Heidenreich PA, Jenkins KJ, Loth AR, Peterson ED, Shahian DM.
PMID: 20889928
Phys Ther. 2010 Oct;90(10):1373-82. doi: 10.1093/ptj/90.10.1373.

No abstract available.

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Thomas RJ, King M, Lui K, et al. Reprint--AACVPR/ACCF/AHA 2010 update: performance measures on cardiac rehabilitation for referral to cardiac rehabilitation/secondary prevention services: a report of the American Association of Cardiovascular and Pulmonary Rehabilitation and the American College of Cardiology Foundation/American Heart Association Task Force on Performance Measures (Writing Committee to Develop Clinical Performance Measures for Cardiac Rehabilitation). Phys Ther. 2010;90(10):1373-82doi: 10.1093/ptj/90.10.1373.
Thomas, R. J., King, M., Lui, K., Oldridge, N., Piña, I. L., Spertus, J., Masoudi, F. A., DeLong, E., Erwin, J. P., Goff, D. C., Grady, K., Green, L. A., Heidenreich, P. A., Jenkins, K. J., Loth, A. R., Peterson, E. D., Shahian, D. M. (2010). Reprint--AACVPR/ACCF/AHA 2010 update: performance measures on cardiac rehabilitation for referral to cardiac rehabilitation/secondary prevention services: a report of the American Association of Cardiovascular and Pulmonary Rehabilitation and the American College of Cardiology Foundation/American Heart Association Task Force on Performance Measures (Writing Committee to Develop Clinical Performance Measures for Cardiac Rehabilitation). Physical therapy, 90(10), 1373-82. https://doi.org/10.1093/ptj/90.10.1373
Thomas, Randal J, et al. "Reprint--AACVPR/ACCF/AHA 2010 update: performance measures on cardiac rehabilitation for referral to cardiac rehabilitation/secondary prevention services: a report of the American Association of Cardiovascular and Pulmonary Rehabilitation and the American College of Cardiology Foundation/American Heart Association Task Force on Performance Measures (Writing Committee to Develop Clinical Performance Measures for Cardiac Rehabilitation)." Physical therapy vol. 90,10 (2010): 1373-82. doi: https://doi.org/10.1093/ptj/90.10.1373
Thomas RJ, King M, Lui K, Oldridge N, Piña IL, Spertus J, Masoudi FA, DeLong E, Erwin JP, Goff DC, Grady K, Green LA, Heidenreich PA, Jenkins KJ, Loth AR, Peterson ED, Shahian DM. Reprint--AACVPR/ACCF/AHA 2010 update: performance measures on cardiac rehabilitation for referral to cardiac rehabilitation/secondary prevention services: a report of the American Association of Cardiovascular and Pulmonary Rehabilitation and the American College of Cardiology Foundation/American Heart Association Task Force on Performance Measures (Writing Committee to Develop Clinical Performance Measures for Cardiac Rehabilitation). Phys Ther. 2010 Oct;90(10):1373-82. doi: 10.1093/ptj/90.10.1373. PMID: 20889928.
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The Pathology and Chemistry of Experimental OEdema in the Brain.

Proceedings of the Royal Society of Medicine

Aldridge WN.
PMID: 19994442
Proc R Soc Med. 1965 Aug;58(8):599.

No abstract available.

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Aldridge WN. The Pathology and Chemistry of Experimental OEdema in the Brain. Proc R Soc Med. 1965;58(8):599
Aldridge, W. N. (1965). The Pathology and Chemistry of Experimental OEdema in the Brain. Proceedings of the Royal Society of Medicine, 58(8), 599.
Aldridge, W N. "The Pathology and Chemistry of Experimental OEdema in the Brain." Proceedings of the Royal Society of Medicine vol. 58,8 (1965): 599.
Aldridge WN. The Pathology and Chemistry of Experimental OEdema in the Brain. Proc R Soc Med. 1965 Aug;58(8):599. PMID: 19994442; PMCID: PMC1898851.
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The use of videoconferencing to enhance interprofessional clinical education for allied health students.

Journal of interprofessional care

Britt KL, Hewish S, Rodda J, Eldridge B.
PMID: 22458640
J Interprof Care. 2012 Jul;26(4):333-5. doi: 10.3109/13561820.2012.671385. Epub 2012 Mar 29.

The Health-e-Learning project investigated the use of videoconferencing to deliver interprofessional clinical education to allied health students. Via a broadband link, students observed DVD footage of a clinical session then participated in discussion with the clinicians at the Royal...

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Britt KL, Hewish S, Rodda J, et al. The use of videoconferencing to enhance interprofessional clinical education for allied health students. J Interprof Care. 2012;26(4):333-5doi: 10.3109/13561820.2012.671385.
Britt, K. L., Hewish, S., Rodda, J., & Eldridge, B. (2012). The use of videoconferencing to enhance interprofessional clinical education for allied health students. Journal of interprofessional care, 26(4), 333-5. https://doi.org/10.3109/13561820.2012.671385
Britt, Kerry Lee, et al. "The use of videoconferencing to enhance interprofessional clinical education for allied health students." Journal of interprofessional care vol. 26,4 (2012): 333-5. doi: https://doi.org/10.3109/13561820.2012.671385
Britt KL, Hewish S, Rodda J, Eldridge B. The use of videoconferencing to enhance interprofessional clinical education for allied health students. J Interprof Care. 2012 Jul;26(4):333-5. doi: 10.3109/13561820.2012.671385. Epub 2012 Mar 29. PMID: 22458640.
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Photophysical characterization of light-emitting poly(indenofluorene)s.

Chemphyschem : a European journal of chemical physics and physical chemistry

Keivanidis PE, Jacob J, Oldridge L, Sonar P, Carbonnier B, Baluschev S, Grimsdale AC, Müllen K, Wegner G.
PMID: 16082667
Chemphyschem. 2005 Aug 12;6(8):1650-60. doi: 10.1002/cphc.200400634.

Time-resolved photoluminescence spectroscopy experiments of three poly(2,8-indenofluorene) derivatives bearing different pendant groups are presented. A comparison of the photophysical properties of dilute solutions and thin films provides information on the chemical purity of the materials. The photophysical properties of...

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Keivanidis PE, Jacob J, Oldridge L, et al. Photophysical characterization of light-emitting poly(indenofluorene)s. Chemphyschem. 2005;6(8):1650-60doi: 10.1002/cphc.200400634.
Keivanidis, P. E., Jacob, J., Oldridge, L., Sonar, P., Carbonnier, B., Baluschev, S., Grimsdale, A. C., Müllen, K., & Wegner, G. (2005). Photophysical characterization of light-emitting poly(indenofluorene)s. Chemphyschem : a European journal of chemical physics and physical chemistry, 6(8), 1650-60. https://doi.org/10.1002/cphc.200400634
Keivanidis, Panagiotis E, et al. "Photophysical characterization of light-emitting poly(indenofluorene)s." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 6,8 (2005): 1650-60. doi: https://doi.org/10.1002/cphc.200400634
Keivanidis PE, Jacob J, Oldridge L, Sonar P, Carbonnier B, Baluschev S, Grimsdale AC, Müllen K, Wegner G. Photophysical characterization of light-emitting poly(indenofluorene)s. Chemphyschem. 2005 Aug 12;6(8):1650-60. doi: 10.1002/cphc.200400634. PMID: 16082667.
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Evaluation of electronics, electrostatics and hydrogen bond cooperativity in the binding of cyanide and fluoride by Lewis acidic ferrocenylboranes.

Inorganic chemistry

Broomsgrove AE, Addy DA, Di Paolo A, Morgan IR, Bresner C, Chislett V, Fallis IA, Thompson AL, Vidovic D, Aldridge S.
PMID: 19957927
Inorg Chem. 2010 Jan 04;49(1):157-73. doi: 10.1021/ic901673u.

Synthetic approaches based on the direct borylation of ferrocene by BBr(3), followed by boryl substituent modification, or on the lithiation of ferrocene derivatives and subsequent quenching with the electrophile FBMes(2), have given access to a range of ferrocene derivatized...

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Broomsgrove AE, Addy DA, Di Paolo A, et al. Evaluation of electronics, electrostatics and hydrogen bond cooperativity in the binding of cyanide and fluoride by Lewis acidic ferrocenylboranes. Inorg Chem. 2010;49(1):157-73doi: 10.1021/ic901673u.
Broomsgrove, A. E., Addy, D. A., Di Paolo, A., Morgan, I. R., Bresner, C., Chislett, V., Fallis, I. A., Thompson, A. L., Vidovic, D., & Aldridge, S. (2010). Evaluation of electronics, electrostatics and hydrogen bond cooperativity in the binding of cyanide and fluoride by Lewis acidic ferrocenylboranes. Inorganic chemistry, 49(1), 157-73. https://doi.org/10.1021/ic901673u
Broomsgrove, Alexander E J, et al. "Evaluation of electronics, electrostatics and hydrogen bond cooperativity in the binding of cyanide and fluoride by Lewis acidic ferrocenylboranes." Inorganic chemistry vol. 49,1 (2010): 157-73. doi: https://doi.org/10.1021/ic901673u
Broomsgrove AE, Addy DA, Di Paolo A, Morgan IR, Bresner C, Chislett V, Fallis IA, Thompson AL, Vidovic D, Aldridge S. Evaluation of electronics, electrostatics and hydrogen bond cooperativity in the binding of cyanide and fluoride by Lewis acidic ferrocenylboranes. Inorg Chem. 2010 Jan 04;49(1):157-73. doi: 10.1021/ic901673u. PMID: 19957927.
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High-Performance Silicon Nanopore Hemofiltration Membranes.

Journal of membrane science

Fissell WH, Dubnisheva A, Eldridge AN, Fleischman AJ, Zydney AL, Roy S.
PMID: 20054402
J Memb Sci. 2009 Jan 05;326(1):58-63. doi: 10.1016/j.memsci.2008.09.039.

Silicon micromachining provides the precise control of nanoscale features that can be fundamentally enabling for miniaturized, implantable medical devices. Concerns have been raised regarding blood biocompatibility of silicon-based materials and their application to hemodialysis and hemofiltration. A high-performance ultrathin...

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Fissell WH, Dubnisheva A, Eldridge AN, et al. High-Performance Silicon Nanopore Hemofiltration Membranes. J Memb Sci. 2009;326(1):58-63doi: 10.1016/j.memsci.2008.09.039.
Fissell, W. H., Dubnisheva, A., Eldridge, A. N., Fleischman, A. J., Zydney, A. L., & Roy, S. (2009). High-Performance Silicon Nanopore Hemofiltration Membranes. Journal of membrane science, 326(1), 58-63. https://doi.org/10.1016/j.memsci.2008.09.039
Fissell, William H, et al. "High-Performance Silicon Nanopore Hemofiltration Membranes." Journal of membrane science vol. 326,1 (2009): 58-63. doi: https://doi.org/10.1016/j.memsci.2008.09.039
Fissell WH, Dubnisheva A, Eldridge AN, Fleischman AJ, Zydney AL, Roy S. High-Performance Silicon Nanopore Hemofiltration Membranes. J Memb Sci. 2009 Jan 05;326(1):58-63. doi: 10.1016/j.memsci.2008.09.039. PMID: 20054402; PMCID: PMC2607036.
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Sliding away from PowerPoint: the interactive lecture.

Nurse educator

Moellenberg KK, Aldridge M.
PMID: 20975416
Nurse Educ. 2010 Nov-Dec;35(6):268-72. doi: 10.1097/NNE.0b013e3181f7f2f7.

Class participation can be difficult to obtain when lecturing to a large group of students. Interactive lecture methods can help bridge the gap between faculty and students as well as increase class participation and satisfaction among faculty and students....

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Moellenberg KK, Aldridge M. Sliding away from PowerPoint: the interactive lecture. Nurse Educ. 2010;35(6):268-72doi: 10.1097/NNE.0b013e3181f7f2f7.
Moellenberg, K. K., & Aldridge, M. (2010). Sliding away from PowerPoint: the interactive lecture. Nurse educator, 35(6), 268-72. https://doi.org/10.1097/NNE.0b013e3181f7f2f7
Moellenberg, Kara K, and Aldridge, Michael. "Sliding away from PowerPoint: the interactive lecture." Nurse educator vol. 35,6 (2010): 268-72. doi: https://doi.org/10.1097/NNE.0b013e3181f7f2f7
Moellenberg KK, Aldridge M. Sliding away from PowerPoint: the interactive lecture. Nurse Educ. 2010 Nov-Dec;35(6):268-72. doi: 10.1097/NNE.0b013e3181f7f2f7. PMID: 20975416.
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Bulky guanidinato and amidinato zinc complexes and their comparative stabilities.

Dalton transactions (Cambridge, England : 2003)

Jones C, Furness L, Nembenna S, Rose RP, Aldridge S, Stasch A.
PMID: 20714636
Dalton Trans. 2010 Oct 07;39(37):8788-95. doi: 10.1039/c0dt00589d. Epub 2010 Aug 12.

The preparation of a series of amidinato and guanidinato zinc halide complexes incorporating ligands of varying steric bulk is described, and their thermal stabilities compared. Salt elimination reactions between [M(Giso)] (M = K or Li; Giso = [(ArN)(2)CNCy(2)](-), Ar...

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Jones C, Furness L, Nembenna S, et al. Bulky guanidinato and amidinato zinc complexes and their comparative stabilities. Dalton Trans. 2010;39(37):8788-95doi: 10.1039/c0dt00589d.
Jones, C., Furness, L., Nembenna, S., Rose, R. P., Aldridge, S., & Stasch, A. (2010). Bulky guanidinato and amidinato zinc complexes and their comparative stabilities. Dalton transactions (Cambridge, England : 2003), 39(37), 8788-95. https://doi.org/10.1039/c0dt00589d
Jones, Cameron, et al. "Bulky guanidinato and amidinato zinc complexes and their comparative stabilities." Dalton transactions (Cambridge, England : 2003) vol. 39,37 (2010): 8788-95. doi: https://doi.org/10.1039/c0dt00589d
Jones C, Furness L, Nembenna S, Rose RP, Aldridge S, Stasch A. Bulky guanidinato and amidinato zinc complexes and their comparative stabilities. Dalton Trans. 2010 Oct 07;39(37):8788-95. doi: 10.1039/c0dt00589d. Epub 2010 Aug 12. PMID: 20714636.
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Al-H σ-bond coordination: expanded ring carbene adducts of AlH3 as neutral bi- and tri-functional donor ligands.

Chemical communications (Cambridge, England)

Abdalla JA, Riddlestone IM, Tirfoin R, Phillips N, Bates JI, Aldridge S.
PMID: 23673812
Chem Commun (Camb). 2013 Jun 21;49(49):5547-9. doi: 10.1039/c3cc42342e.

Thermally robust expanded ring carbene adducts of AlH3 have been synthesized with a view to probing their ligating abilities via Al-H σ-bond coordination. While κ(2) binding to the 14-electron [Mo(CO)4] fragment is readily demonstrated, interaction with [Mo(CO)3] results in...

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Abdalla JA, Riddlestone IM, Tirfoin R, et al. Al-H σ-bond coordination: expanded ring carbene adducts of AlH3 as neutral bi- and tri-functional donor ligands. Chem Commun (Camb). 2013;49(49):5547-9doi: 10.1039/c3cc42342e.
Abdalla, J. A., Riddlestone, I. M., Tirfoin, R., Phillips, N., Bates, J. I., & Aldridge, S. (2013). Al-H σ-bond coordination: expanded ring carbene adducts of AlH3 as neutral bi- and tri-functional donor ligands. Chemical communications (Cambridge, England), 49(49), 5547-9. https://doi.org/10.1039/c3cc42342e
Abdalla, Joseph A B, et al. "Al-H σ-bond coordination: expanded ring carbene adducts of AlH3 as neutral bi- and tri-functional donor ligands." Chemical communications (Cambridge, England) vol. 49,49 (2013): 5547-9. doi: https://doi.org/10.1039/c3cc42342e
Abdalla JA, Riddlestone IM, Tirfoin R, Phillips N, Bates JI, Aldridge S. Al-H σ-bond coordination: expanded ring carbene adducts of AlH3 as neutral bi- and tri-functional donor ligands. Chem Commun (Camb). 2013 Jun 21;49(49):5547-9. doi: 10.1039/c3cc42342e. PMID: 23673812.
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Probing the limits of ligand steric bulk: backbone C-H activation in a saturated N-heterocyclic carbene.

Chemistry (Weinheim an der Bergstrasse, Germany)

Phillips N, Tirfoin R, Aldridge S.
PMID: 24616039
Chemistry. 2014 Mar 24;20(13):3825-30. doi: 10.1002/chem.201304243. Epub 2014 Feb 24.

The consequences of extremely high steric loading have been probed for late transition metal complexes featuring the expanded ring N-heterocyclic carbene 6-Dipp. The reluctance of this ligand to form 2:1 complexes with d-block metals (rationalised on the basis of...

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Phillips N, Tirfoin R, Aldridge S. Probing the limits of ligand steric bulk: backbone C-H activation in a saturated N-heterocyclic carbene. Chemistry. 2014;20(13):3825-30doi: 10.1002/chem.201304243.
Phillips, N., Tirfoin, R., & Aldridge, S. (2014). Probing the limits of ligand steric bulk: backbone C-H activation in a saturated N-heterocyclic carbene. Chemistry (Weinheim an der Bergstrasse, Germany), 20(13), 3825-30. https://doi.org/10.1002/chem.201304243
Phillips, Nicholas, et al. "Probing the limits of ligand steric bulk: backbone C-H activation in a saturated N-heterocyclic carbene." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 20,13 (2014): 3825-30. doi: https://doi.org/10.1002/chem.201304243
Phillips N, Tirfoin R, Aldridge S. Probing the limits of ligand steric bulk: backbone C-H activation in a saturated N-heterocyclic carbene. Chemistry. 2014 Mar 24;20(13):3825-30. doi: 10.1002/chem.201304243. Epub 2014 Feb 24. PMID: 24616039.
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Showing 13 to 24 of 389 entries